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Akums Lifesciences Limited

Alkaloids Unit 1

Angelini Pharmaceuticals ACRAF

Anuh Pharma LTD

Apothecon Pharmaceuticals

Bachem AG

Bachem Americas, Inc

Bachem Americas, Inc.

Bachem SA, Succursale de Vionnaz

Bio-gen Extracts Pvt. Ltd.

Bloomage Biotechnology Corp., Ltd

Bloomage Freda Biopharm Co.,Ltd.

Bora Pharmaceutical Services Inc.

CAD Middle East Pharmaceutical Industries LLC

Cebiphar

Century Pharmaceuticals

Changzhou Pharmaceutical Factory

Curia Wisconsin Inc.

Curtec International

Dabur Research Foundation

Deccan Nutraceuticals Pvt. Ltd.

Enaltec Labs Private Limited

Ethypharm

Ethypharm Inc

Eurofarma Laboratorios S.A.

Farbe Firma

Farmak A.S

Farmak A.S.

Global Pharmatech Pvt. Ltd

Health Biotech

Health Biotech Limited

Heilen Biopharm Pvt. Ltd

Hiranya Cellulose Products

ICBio Clinical Research Pvt Ltd

Icrom SpA

Interquim SA

JQC Huayin Pharmaceutical Co Ltd

Jetpharma SA

Jiangsu Zhongbang Pharmaceutical Co, Ltd

Kangcare Bioindustry Co.,ltd

LAURUS LABS

Lusochimica SPA

MURLI KRISHNA PHARMA PVT LTD

Medichem Manufacturing Malta Ltd

Medichem S.A.

Meenaxy Pharma Pvt. Ltd

Megafine Pharma (P) Ltd

Megsan Labs Private Limited

Metrochem API Private Limited Unit I

Metrochem API Private Limited Unit I & Unit II

Metrochem API Private Limited Unit IV

Metrochem API Private Limited- Unit-I

Microchem SRL

Minakem High Potent

PIERRE FABRE

PMC Isochem

PROCOS S.p.A.

Peter Greven Nederland C.V

Pharmactive ilac San. ve Tic. A.S.

Phyton Biotech GmbH

Phyton Biotech LLC

Phyton Biotech, GmbH

Rafarm S.A

Ramdev Chemical Pvt Ltd

Reine Lifescience

SANLI ILAC

SM BIOMED SDN. BHD

Sai Tech Pharmaceuticals Pvt Ltd

Shandong Boyuan Pharmaceutical

Shenzhen Oriental Pharmaceutial Co.,Ltd

Shodhana Laboratories Ltd

Stellence Pharmscience Private Limited

Synnat Pharma Pvt. Ltd.

Temad Co., Active Pharmaceutical Ingredients

Titan Laboratories Pvt Ltd.

Trimax Bio Sciences (P) Limited

Unither Pharmaceuticals

VPL CHEMICALS PVT LTD

World Medicine Ilac San ve tic LTD STl

XL Laboratories Private Limited

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Health Canada: Inspection Start Date: 2016-05-20; Type- GMP Foreign Rating- Compliant
PMC Isochem is a CDMO company acquired by PMC International in 2017. It manufactures cGMP intermedia...
PMC Isochem is a CDMO company acquired by PMC International in 2017. It manufactures cGMP intermediates, active pharmaceutical ingredients and functional excipients for pharmaceutical and personal care companies worldwide. Its business includes research, product and process development, pilot-scale, industrial production and regulatory approvals support. It adds value to its clients' intellectual property through constant innovation in manufacturing techniques throughout the product life cycle. PMC Isochem's facilities are located within 60 miles of Paris and are all US FDA-audited plants.

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Health Canada: Inspection Start Date: 2014-01-10; Type- GMP Foreign
PMC Isochem is a CDMO company acquired by PMC International in 2017. It manufactures cGMP intermedia...
PMC Isochem is a CDMO company acquired by PMC International in 2017. It manufactures cGMP intermediates, active pharmaceutical ingredients and functional excipients for pharmaceutical and personal care companies worldwide. Its business includes research, product and process development, pilot-scale, industrial production and regulatory approvals support. It adds value to its clients' intellectual property through constant innovation in manufacturing techniques throughout the product life cycle. PMC Isochem's facilities are located within 60 miles of Paris and are all US FDA-audited plants.

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FDA-China: Approved
Bloomage Biotechnology Corporation Limited (formerly Bloomage Freda Biopharm) was established by the...
Bloomage Biotechnology Corporation Limited (formerly Bloomage Freda Biopharm) was established by the Bloomage International Investment Group. Over the years, it has established itself as a world-renowned manufacturer of bioactive materials. In the 1990s, it became the first company in China to develop the fermentation procedure to manufacture sodium hyaluronate. It has also established around 200 specifications of hyaluronic acid that are used in the pharmaceutical, medical devices, cosmetics and functional foods industry. As a raw material business unit, Bloomage Biotech provides innovative solutions and technical support to its partners.
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FDA-USA: Approved
Bloomage Biotechnology Corporation Limited (formerly Bloomage Freda Biopharm) was established by the...
Bloomage Biotechnology Corporation Limited (formerly Bloomage Freda Biopharm) was established by the Bloomage International Investment Group. Over the years, it has established itself as a world-renowned manufacturer of bioactive materials. In the 1990s, it became the first company in China to develop the fermentation procedure to manufacture sodium hyaluronate. It has also established around 200 specifications of hyaluronic acid that are used in the pharmaceutical, medical devices, cosmetics and functional foods industry. As a raw material business unit, Bloomage Biotech provides innovative solutions and technical support to its partners.
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MFDS- Korea: Approved
Bloomage Biotechnology Corporation Limited (formerly Bloomage Freda Biopharm) was established by the...
Bloomage Biotechnology Corporation Limited (formerly Bloomage Freda Biopharm) was established by the Bloomage International Investment Group. Over the years, it has established itself as a world-renowned manufacturer of bioactive materials. In the 1990s, it became the first company in China to develop the fermentation procedure to manufacture sodium hyaluronate. It has also established around 200 specifications of hyaluronic acid that are used in the pharmaceutical, medical devices, cosmetics and functional foods industry. As a raw material business unit, Bloomage Biotech provides innovative solutions and technical support to its partners.
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GMP Certificate-SD150009
Bloomage Biotechnology Corporation Limited (formerly Bloomage Freda Biopharm) was established by the...
Bloomage Biotechnology Corporation Limited (formerly Bloomage Freda Biopharm) was established by the Bloomage International Investment Group. Over the years, it has established itself as a world-renowned manufacturer of bioactive materials. In the 1990s, it became the first company in China to develop the fermentation procedure to manufacture sodium hyaluronate. It has also established around 200 specifications of hyaluronic acid that are used in the pharmaceutical, medical devices, cosmetics and functional foods industry. As a raw material business unit, Bloomage Biotech provides innovative solutions and technical support to its partners.
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PMDA-Japan: Approved
Bloomage Biotechnology Corporation Limited (formerly Bloomage Freda Biopharm) was established by the...
Bloomage Biotechnology Corporation Limited (formerly Bloomage Freda Biopharm) was established by the Bloomage International Investment Group. Over the years, it has established itself as a world-renowned manufacturer of bioactive materials. In the 1990s, it became the first company in China to develop the fermentation procedure to manufacture sodium hyaluronate. It has also established around 200 specifications of hyaluronic acid that are used in the pharmaceutical, medical devices, cosmetics and functional foods industry. As a raw material business unit, Bloomage Biotech provides innovative solutions and technical support to its partners.
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FDA- USA:GMP Audit
Minakem is a fully integrated development partner and commercial manufacturer for pharma companies. ...
Minakem is a fully integrated development partner and commercial manufacturer for pharma companies. With around 70 years of experience, Minakem is a technology-driven company with expertise in complex multi-step synthesis, pressure chemistry, chiral synthesis, halogenation chemistry, steroid chemistry and prazole chemistry. It offers custom development & manufacturing, API manufacturing and the production of key intermediates. Minakem has 3 USFDA-approved development and manufacturing sites in France and Belgium. Minakem is an affiliate of the Minafin Group and has access to all technologies, resources, and capabilities.

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FAMHP- Belgium
Minakem is a fully integrated development partner and commercial manufacturer for pharma companies. ...
Minakem is a fully integrated development partner and commercial manufacturer for pharma companies. With around 70 years of experience, Minakem is a technology-driven company with expertise in complex multi-step synthesis, pressure chemistry, chiral synthesis, halogenation chemistry, steroid chemistry and prazole chemistry. It offers custom development & manufacturing, API manufacturing and the production of key intermediates. Minakem has 3 USFDA-approved development and manufacturing sites in France and Belgium. Minakem is an affiliate of the Minafin Group and has access to all technologies, resources, and capabilities.

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USFDA - 2016
Farmak, A.S. is a privately held chemical and pharmaceutical company based in the Czech Republic. It...
Farmak, A.S. is a privately held chemical and pharmaceutical company based in the Czech Republic. It specializes in researching, developing and producing active pharmaceutical ingredients (APIs), intermediates and specialized chemicals. The company primarily focuses on exporting its products, with the main markets being the EU, USA, India, Japan and Latin America. Additionally, Farmak offers contract manufacturing and custom synthesis services through its R&D department to support the clients.

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PMDA- Japan
Farmak, A.S. is a privately held chemical and pharmaceutical company based in the Czech Republic. It...
Farmak, A.S. is a privately held chemical and pharmaceutical company based in the Czech Republic. It specializes in researching, developing and producing active pharmaceutical ingredients (APIs), intermediates and specialized chemicals. The company primarily focuses on exporting its products, with the main markets being the EU, USA, India, Japan and Latin America. Additionally, Farmak offers contract manufacturing and custom synthesis services through its R&D department to support the clients.

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USFDA - 2018
Farmak, A.S. is a privately held chemical and pharmaceutical company based in the Czech Republic. It...
Farmak, A.S. is a privately held chemical and pharmaceutical company based in the Czech Republic. It specializes in researching, developing and producing active pharmaceutical ingredients (APIs), intermediates and specialized chemicals. The company primarily focuses on exporting its products, with the main markets being the EU, USA, India, Japan and Latin America. Additionally, Farmak offers contract manufacturing and custom synthesis services through its R&D department to support the clients.

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Health Canada: Reference Number: 506546; Inspection Start Date: 2016-10-18; Type- GMP Domestic - Reg...
Health Canada: Reference Number: 506546; Inspection Start Date: 2016-10-18; Type- GMP Domestic - Regular Inspection
Phyton Biotech, a division of DFB Pharmaceuticals, was founded in 1990. Using its Plant Cell Ferment...
Phyton Biotech, a division of DFB Pharmaceuticals, was founded in 1990. Using its Plant Cell Fermentation (PCF) technology, Phyton Biotech is currently the world’s largest producer of high-quality paclitaxel and docetaxel. It offers clients a full range of integrated contract product and process development and commercial manufacturing services across the entire development chain, from feasibility to commercial production, to the pharmaceutical, cosmetic, agricultural and food ingredient industries. Its facilities in Germany and Canada have been inspected by multiple regulatory agencies and comply with international GMP requirements.

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Health Canada: Reference Number: 506546; Inspection Start Date: 2014-10-07; Type- GMP Domestic - Ini...
Health Canada: Reference Number: 506546; Inspection Start Date: 2014-10-07; Type- GMP Domestic - Initial Inspection
Phyton Biotech, a division of DFB Pharmaceuticals, was founded in 1990. Using its Plant Cell Ferment...
Phyton Biotech, a division of DFB Pharmaceuticals, was founded in 1990. Using its Plant Cell Fermentation (PCF) technology, Phyton Biotech is currently the world’s largest producer of high-quality paclitaxel and docetaxel. It offers clients a full range of integrated contract product and process development and commercial manufacturing services across the entire development chain, from feasibility to commercial production, to the pharmaceutical, cosmetic, agricultural and food ingredient industries. Its facilities in Germany and Canada have been inspected by multiple regulatory agencies and comply with international GMP requirements.

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Health Canada: Reference Number: 508839; Inspection Start Date: 2014-03-20; Type- GMP Foreign
Phyton Biotech, a division of DFB Pharmaceuticals, was founded in 1990. Using its Plant Cell Ferment...
Phyton Biotech, a division of DFB Pharmaceuticals, was founded in 1990. Using its Plant Cell Fermentation (PCF) technology, Phyton Biotech is currently the world’s largest producer of high-quality paclitaxel and docetaxel. It offers clients a full range of integrated contract product and process development and commercial manufacturing services across the entire development chain, from feasibility to commercial production, to the pharmaceutical, cosmetic, agricultural and food ingredient industries. Its facilities in Germany and Canada have been inspected by multiple regulatory agencies and comply with international GMP requirements.

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Korean FDA: June 2012
Phyton Biotech, a division of DFB Pharmaceuticals, was founded in 1990. Using its Plant Cell Ferment...
Phyton Biotech, a division of DFB Pharmaceuticals, was founded in 1990. Using its Plant Cell Fermentation (PCF) technology, Phyton Biotech is currently the world’s largest producer of high-quality paclitaxel and docetaxel. It offers clients a full range of integrated contract product and process development and commercial manufacturing services across the entire development chain, from feasibility to commercial production, to the pharmaceutical, cosmetic, agricultural and food ingredient industries. Its facilities in Germany and Canada have been inspected by multiple regulatory agencies and comply with international GMP requirements.

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TGA: August 2010
Phyton Biotech, a division of DFB Pharmaceuticals, was founded in 1990. Using its Plant Cell Ferment...
Phyton Biotech, a division of DFB Pharmaceuticals, was founded in 1990. Using its Plant Cell Fermentation (PCF) technology, Phyton Biotech is currently the world’s largest producer of high-quality paclitaxel and docetaxel. It offers clients a full range of integrated contract product and process development and commercial manufacturing services across the entire development chain, from feasibility to commercial production, to the pharmaceutical, cosmetic, agricultural and food ingredient industries. Its facilities in Germany and Canada have been inspected by multiple regulatory agencies and comply with international GMP requirements.

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Korean FDA: January 2013
Phyton Biotech, a division of DFB Pharmaceuticals, was founded in 1990. Using its Plant Cell Ferment...
Phyton Biotech, a division of DFB Pharmaceuticals, was founded in 1990. Using its Plant Cell Fermentation (PCF) technology, Phyton Biotech is currently the world’s largest producer of high-quality paclitaxel and docetaxel. It offers clients a full range of integrated contract product and process development and commercial manufacturing services across the entire development chain, from feasibility to commercial production, to the pharmaceutical, cosmetic, agricultural and food ingredient industries. Its facilities in Germany and Canada have been inspected by multiple regulatory agencies and comply with international GMP requirements.

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swissmedic- GMP
With more than 50 years of experience and expertise, Bachem provides products for research, clinical...
With more than 50 years of experience and expertise, Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide, providing a wide range of services. Over the years, Bachem has established itself as a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. The company is headquartered in Switzerland and has offices in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange.

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Health Canada: Inspection Start Date: 2015-06-17; Type- GMP Foreign
With more than 50 years of experience and expertise, Bachem provides products for research, clinical...
With more than 50 years of experience and expertise, Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide, providing a wide range of services. Over the years, Bachem has established itself as a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. The company is headquartered in Switzerland and has offices in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange.

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Health Canada: Inspection Start Date: 2014-11-03; Type- GMP Foreign
With more than 50 years of experience and expertise, Bachem provides products for research, clinical...
With more than 50 years of experience and expertise, Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide, providing a wide range of services. Over the years, Bachem has established itself as a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. The company is headquartered in Switzerland and has offices in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange.

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Health Canada: Inspection Start Date: 2014-11-03; Type- GMP Foreign
With more than 50 years of experience and expertise, Bachem provides products for research, clinical...
With more than 50 years of experience and expertise, Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide, providing a wide range of services. Over the years, Bachem has established itself as a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. The company is headquartered in Switzerland and has offices in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange.

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Health Canada: Inspection Start Date: 2013-01-22; Type- GMP Foreign
With more than 50 years of experience and expertise, Bachem provides products for research, clinical...
With more than 50 years of experience and expertise, Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide, providing a wide range of services. Over the years, Bachem has established itself as a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. The company is headquartered in Switzerland and has offices in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange.

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Health Canada: Inspection Start Date: 2012-04-24; Type- GMP Foreign
With more than 50 years of experience and expertise, Bachem provides products for research, clinical...
With more than 50 years of experience and expertise, Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide, providing a wide range of services. Over the years, Bachem has established itself as a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. The company is headquartered in Switzerland and has offices in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange.

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Health Canada: Inspection Start Date: 2012-04-16; Type- GMP Foreign
With more than 50 years of experience and expertise, Bachem provides products for research, clinical...
With more than 50 years of experience and expertise, Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide, providing a wide range of services. Over the years, Bachem has established itself as a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. The company is headquartered in Switzerland and has offices in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange.

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Health Canada: Inspection Start Date: 2012-01-09; Type- GMP Foreign
With more than 50 years of experience and expertise, Bachem provides products for research, clinical...
With more than 50 years of experience and expertise, Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide, providing a wide range of services. Over the years, Bachem has established itself as a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. The company is headquartered in Switzerland and has offices in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange.

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Health Canada: Inspection Start Date: 2017-05-29; Type- GMP Foreign
Interquim, founded in 1978, is now part of the Ferrer HealthTech division. Interquim specializes in ...
Interquim, founded in 1978, is now part of the Ferrer HealthTech division. Interquim specializes in the development of competitive processes for manufacturing high added-value APIs that meet stringent quality standards. Complying with European environmental and work safety regulations, Interquim’s products are exported to highly regulated pharmaceutical markets. Regulatory bodies and clients have approved its quality system and facilities. With state-of-the-art multi-production plants, drug synthesis, and quality-control labs, Interquim supports clients throughout the entire product lifecycle, from product development to marketing.

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Health Canada: Inspection Start Date: 2016-05-02; Type- GMP Foreign
Interquim, founded in 1978, is now part of the Ferrer HealthTech division. Interquim specializes in ...
Interquim, founded in 1978, is now part of the Ferrer HealthTech division. Interquim specializes in the development of competitive processes for manufacturing high added-value APIs that meet stringent quality standards. Complying with European environmental and work safety regulations, Interquim’s products are exported to highly regulated pharmaceutical markets. Regulatory bodies and clients have approved its quality system and facilities. With state-of-the-art multi-production plants, drug synthesis, and quality-control labs, Interquim supports clients throughout the entire product lifecycle, from product development to marketing.

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Health Canada: Inspection Start Date: 2015-10-29; Type- GMP Foreign
Interquim, founded in 1978, is now part of the Ferrer HealthTech division. Interquim specializes in ...
Interquim, founded in 1978, is now part of the Ferrer HealthTech division. Interquim specializes in the development of competitive processes for manufacturing high added-value APIs that meet stringent quality standards. Complying with European environmental and work safety regulations, Interquim’s products are exported to highly regulated pharmaceutical markets. Regulatory bodies and clients have approved its quality system and facilities. With state-of-the-art multi-production plants, drug synthesis, and quality-control labs, Interquim supports clients throughout the entire product lifecycle, from product development to marketing.

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GMP Certificate
Established in 1997, Temad Co. is one of the largest producers of APIs in Iran & an innovative manuf...
Established in 1997, Temad Co. is one of the largest producers of APIs in Iran & an innovative manufacturer of narcotic and non-narcotic products of world-class quality in the Middle East. Apart from complying with Iranian GMP regulations, Temad has acquired the national & international standards of API manufacturing such as ISO 9001/14001/17025/45001 and OHSAS 18001. It currently manufactures more than 115 pharmaceutical products, including narcotics and non-narcotics, in accordance with GMP and WHO standards and regulations. Temad exports its products to 45 countries worldwide.
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GMP Certificate
Century Pharmaceuticals, established in 1982, has 40 years of experience in manufacturing APIs. It h...
Century Pharmaceuticals, established in 1982, has 40 years of experience in manufacturing APIs. It has been supplying APIs produced in-house to several major pharma companies in India and abroad. Its APIs are manufactured in accordance with cGMP, 21CFR part 10 and ICH guidelines. It also produces intermediates and develops new APIs as per the needs of its clients. Century conducts biotechnological research that focuses on human therapeutic proteins. Currently, research is underway to find treatments for asthma, mastocytosis and basophilic leukemia. Century supplies research-grade biotech products and a wide range of animal health products.

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COFEPRIS: Approved on Dec-2012
Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manuf...
Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manufacturers. It has 6 dedicated manufacturing facilities for its 3 core product groups and has been approved by ISO 9001-2015, USFDA, WHO GMP, Cofepris & Japanese authorities. Metrochem’s in-depth industry knowledge, & hi-tech & advanced infrastructure, helps it provide quality products to its customers.

Note: None of the products will be supplied to the countries where this could conflict with existing patents. Further, any products under patent will be offered for R&D purposes only. However, the final responsibility lies with the buyer.

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MFDS: Approved on Feb-2014
Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manuf...
Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manufacturers. It has 6 dedicated manufacturing facilities for its 3 core product groups and has been approved by ISO 9001-2015, USFDA, WHO GMP, Cofepris & Japanese authorities. Metrochem’s in-depth industry knowledge, & hi-tech & advanced infrastructure, helps it provide quality products to its customers.

Note: None of the products will be supplied to the countries where this could conflict with existing patents. Further, any products under patent will be offered for R&D purposes only. However, the final responsibility lies with the buyer.

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WHO GMP: Approved on Oct-2017
Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manuf...
Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manufacturers. It has 6 dedicated manufacturing facilities for its 3 core product groups and has been approved by ISO 9001-2015, USFDA, WHO GMP, Cofepris & Japanese authorities. Metrochem’s in-depth industry knowledge, & hi-tech & advanced infrastructure, helps it provide quality products to its customers.

Note: None of the products will be supplied to the countries where this could conflict with existing patents. Further, any products under patent will be offered for R&D purposes only. However, the final responsibility lies with the buyer.

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PMDA: Approved on May 2019
Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manuf...
Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manufacturers. It has 6 dedicated manufacturing facilities for its 3 core product groups and has been approved by ISO 9001-2015, USFDA, WHO GMP, Cofepris & Japanese authorities. Metrochem’s in-depth industry knowledge, & hi-tech & advanced infrastructure, helps it provide quality products to its customers.

Note: None of the products will be supplied to the countries where this could conflict with existing patents. Further, any products under patent will be offered for R&D purposes only. However, the final responsibility lies with the buyer.

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WHO GMP (Renewal): Approved on Feb 2020
Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manuf...
Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manufacturers. It has 6 dedicated manufacturing facilities for its 3 core product groups and has been approved by ISO 9001-2015, USFDA, WHO GMP, Cofepris & Japanese authorities. Metrochem’s in-depth industry knowledge, & hi-tech & advanced infrastructure, helps it provide quality products to its customers.

Note: None of the products will be supplied to the countries where this could conflict with existing patents. Further, any products under patent will be offered for R&D purposes only. However, the final responsibility lies with the buyer.

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WHO GMP (Fresh): Approved on August 2020
Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manuf...
Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manufacturers. It has 6 dedicated manufacturing facilities for its 3 core product groups and has been approved by ISO 9001-2015, USFDA, WHO GMP, Cofepris & Japanese authorities. Metrochem’s in-depth industry knowledge, & hi-tech & advanced infrastructure, helps it provide quality products to its customers.

Note: None of the products will be supplied to the countries where this could conflict with existing patents. Further, any products under patent will be offered for R&D purposes only. However, the final responsibility lies with the buyer.

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Health Canada
Bora Pharmaceuticals is a premier international contract development and manufacturing organization ...
Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing and packaging of complex oral solid dose, liquid and semi-solid pharmaceutical Rx and OTC products for clinical and commercial uses. From cell-line development and formulation to analytical services and clinical cGMP manufacturing, Bora now provides tailored development and manufacturing services to biologics developers. Bora operates six cGMP manufacturing sites in Asia and North America and delivers to over 100 markets worldwide.
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Integrated Management Systems (IMS) Certificate
Synnat Pharma is a fast-growing pharmaceutical company dedicated to the identification, development,...
Synnat Pharma is a fast-growing pharmaceutical company dedicated to the identification, development, production and distribution of potent phytochemicals and botanical extracts. APIs manufactured by Synnat are used by major drug formulators worldwide. Manufacturing activities are carried out as per ICH cGMP guidelines and several conventional and modern techniques are used for the isolation, semi-synthesis and purification of its products. Synnat Pharma has a presence in semi-regulated and non-regulated markets and is now entering regulated markets.

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State GMP- Visakhapatnam
Synnat Pharma is a fast-growing pharmaceutical company dedicated to the identification, development,...
Synnat Pharma is a fast-growing pharmaceutical company dedicated to the identification, development, production and distribution of potent phytochemicals and botanical extracts. APIs manufactured by Synnat are used by major drug formulators worldwide. Manufacturing activities are carried out as per ICH cGMP guidelines and several conventional and modern techniques are used for the isolation, semi-synthesis and purification of its products. Synnat Pharma has a presence in semi-regulated and non-regulated markets and is now entering regulated markets.

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License Retention Certificate- L.Dis.No.294/AP/DCA/2018
Synnat Pharma is a fast-growing pharmaceutical company dedicated to the identification, development,...
Synnat Pharma is a fast-growing pharmaceutical company dedicated to the identification, development, production and distribution of potent phytochemicals and botanical extracts. APIs manufactured by Synnat are used by major drug formulators worldwide. Manufacturing activities are carried out as per ICH cGMP guidelines and several conventional and modern techniques are used for the isolation, semi-synthesis and purification of its products. Synnat Pharma has a presence in semi-regulated and non-regulated markets and is now entering regulated markets.

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Health Canada: Inspection Start Date: 12-04-2016; Rating- Compliant; Reference No- 508715; Type of I...
Health Canada: Inspection Start Date: 12-04-2016; Rating- Compliant; Reference No- 508715; Type of Inspection- GMP Foreign-Initial On-Site Inspection
Megafine, established in 1995, is a privately owned and professionally managed enterprise with its c...
Megafine, established in 1995, is a privately owned and professionally managed enterprise with its corporate office in MUMBAI and two multipurpose manufacturing sites at VAPI & NASHIK in India for APIs & Intermediates. The facilities have been successfully inspected by US-FDA, EDQM, Japan PMDA, Health Canada, TGA Australia, ANVISA Brazil, COFEPRIS Mexico, Korea MFDS & WHO besides being certified for ISO 9001:2008, 14001:2004 & OHSAS 18001:2007. The company focuses on niche molecules for the regulated market globally.
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China Food & Drug Administration
We are one of the well-known manufacturers of key APIs & intermediates in China, with 20 years of ex...
We are one of the well-known manufacturers of key APIs & intermediates in China, with 20 years of experience & presence in 20+ countries. At Boyuan, we are committed to providing high-quality products & services. Formerly known as “Jinan Boyuan Chemical Co., Ltd” & “Shandong Boyuan Chemical Co., Ltd.” Boyuan was founded in June 2001. We have 2 manufacturing plants in the cities of Jiyang & Yucheng in Shandong Province, China & both are in line with the GMP standard, following a strict quality system & conforming with international standards. Boyuan is dedicated to anti-cancer, anti-fungal & other APIs & intermediates associated.
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Shandong Medical Products Administration
We are one of the well-known manufacturers of key APIs & intermediates in China, with 20 years of ex...
We are one of the well-known manufacturers of key APIs & intermediates in China, with 20 years of experience & presence in 20+ countries. At Boyuan, we are committed to providing high-quality products & services. Formerly known as “Jinan Boyuan Chemical Co., Ltd” & “Shandong Boyuan Chemical Co., Ltd.” Boyuan was founded in June 2001. We have 2 manufacturing plants in the cities of Jiyang & Yucheng in Shandong Province, China & both are in line with the GMP standard, following a strict quality system & conforming with international standards. Boyuan is dedicated to anti-cancer, anti-fungal & other APIs & intermediates associated.
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Health Canada- Site A; GMP Domestic-Regular Inspection; Year 2022
Ethypharm is a European pharmaceutical company focused on CNS and Hospital injectables either throug...
Ethypharm is a European pharmaceutical company focused on CNS and Hospital injectables either through direct sales or through D&L.
Ethypharm is also offering contract development and manufacturing (CDMO) services from formulation, clinical to scale up and commercial phases.
Ethypharm is your CDMO partner for sterile forms (Ampoule, PFS, Vials, Lyo) and conventional (complex solid dosage forms and orals), using conventional API and High potent, Narcotics, Controlled drugs.
Our expertise in Flashtab, Tmask, Nanosizing, Multicaps, Transmucosal, and Orodispersible technologies enables us to develop innovative formulations.

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Health Canada- Site FB1; GMP Foreign
Ethypharm is a European pharmaceutical company focused on CNS and Hospital injectables either throug...
Ethypharm is a European pharmaceutical company focused on CNS and Hospital injectables either through direct sales or through D&L.
Ethypharm is also offering contract development and manufacturing (CDMO) services from formulation, clinical to scale up and commercial phases.
Ethypharm is your CDMO partner for sterile forms (Ampoule, PFS, Vials, Lyo) and conventional (complex solid dosage forms and orals), using conventional API and High potent, Narcotics, Controlled drugs.
Our expertise in Flashtab, Tmask, Nanosizing, Multicaps, Transmucosal, and Orodispersible technologies enables us to develop innovative formulations.

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Health Canada: Inspection Start Date: 2016-10-05; Type- GMP Foreign
Medichem is an indepently-owned company based in Barcelona. Founded in 1972 and with more than 45 ye...
Medichem is an indepently-owned company based in Barcelona. Founded in 1972 and with more than 45 years, Medichem has been engaged in the process development and manufacture of Active Pharmaceutical Ingredients (APIs), including Highly Potent. In 2016, Medichem merged with Combino Pharm, which is devoted to the development and manufacture (licensing) of Finished Dosage Forms. With this merger, Medichem has become a vertically integrated pharmaceutical company which can offer a complete range of products and services for the pharmaceutical industry with the highest standards of quality, operational excellence and environment respect.

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Health Canada: Inspection Start Date: 2015-09-11; Type- GMP Foreign
Medichem is an indepently-owned company based in Barcelona. Founded in 1972 and with more than 45 ye...
Medichem is an indepently-owned company based in Barcelona. Founded in 1972 and with more than 45 years, Medichem has been engaged in the process development and manufacture of Active Pharmaceutical Ingredients (APIs), including Highly Potent. In 2016, Medichem merged with Combino Pharm, which is devoted to the development and manufacture (licensing) of Finished Dosage Forms. With this merger, Medichem has become a vertically integrated pharmaceutical company which can offer a complete range of products and services for the pharmaceutical industry with the highest standards of quality, operational excellence and environment respect.

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Health Canada: Inspection Start Date: 2014-06-16; Type- GMP Foreign
Medichem is an indepently-owned company based in Barcelona. Founded in 1972 and with more than 45 ye...
Medichem is an indepently-owned company based in Barcelona. Founded in 1972 and with more than 45 years, Medichem has been engaged in the process development and manufacture of Active Pharmaceutical Ingredients (APIs), including Highly Potent. In 2016, Medichem merged with Combino Pharm, which is devoted to the development and manufacture (licensing) of Finished Dosage Forms. With this merger, Medichem has become a vertically integrated pharmaceutical company which can offer a complete range of products and services for the pharmaceutical industry with the highest standards of quality, operational excellence and environment respect.

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Health Canada: Inspection Start Date: 2013-01-07; Type- GMP Foreign
Medichem is an indepently-owned company based in Barcelona. Founded in 1972 and with more than 45 ye...
Medichem is an indepently-owned company based in Barcelona. Founded in 1972 and with more than 45 years, Medichem has been engaged in the process development and manufacture of Active Pharmaceutical Ingredients (APIs), including Highly Potent. In 2016, Medichem merged with Combino Pharm, which is devoted to the development and manufacture (licensing) of Finished Dosage Forms. With this merger, Medichem has become a vertically integrated pharmaceutical company which can offer a complete range of products and services for the pharmaceutical industry with the highest standards of quality, operational excellence and environment respect.

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Zazibona
Having started operations in 1996, we have two decades of experience sustaining relationships with l...
Having started operations in 1996, we have two decades of experience sustaining relationships with large pharma companies by delivering quality sterile products for the Indian market. We are a company that specializes in Sterile Injectables. Our manufacturing facility has USFDA and EU GMP approvals. We manufacture sterile solutions in vials and ampoules and will have lyophilization capability by March 2021. Right from inception, we have built a reputation as a reliable supplier and partner for sterile injectables Contract Manufacturing.
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Health Canada
Having started operations in 1996, we have two decades of experience sustaining relationships with l...
Having started operations in 1996, we have two decades of experience sustaining relationships with large pharma companies by delivering quality sterile products for the Indian market. We are a company that specializes in Sterile Injectables. Our manufacturing facility has USFDA and EU GMP approvals. We manufacture sterile solutions in vials and ampoules and will have lyophilization capability by March 2021. Right from inception, we have built a reputation as a reliable supplier and partner for sterile injectables Contract Manufacturing.
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ISO 9001
Having started operations in 1996, we have two decades of experience sustaining relationships with l...
Having started operations in 1996, we have two decades of experience sustaining relationships with large pharma companies by delivering quality sterile products for the Indian market. We are a company that specializes in Sterile Injectables. Our manufacturing facility has USFDA and EU GMP approvals. We manufacture sterile solutions in vials and ampoules and will have lyophilization capability by March 2021. Right from inception, we have built a reputation as a reliable supplier and partner for sterile injectables Contract Manufacturing.
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EU GMP Hungary
Having started operations in 1996, we have two decades of experience sustaining relationships with l...
Having started operations in 1996, we have two decades of experience sustaining relationships with large pharma companies by delivering quality sterile products for the Indian market. We are a company that specializes in Sterile Injectables. Our manufacturing facility has USFDA and EU GMP approvals. We manufacture sterile solutions in vials and ampoules and will have lyophilization capability by March 2021. Right from inception, we have built a reputation as a reliable supplier and partner for sterile injectables Contract Manufacturing.
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PIC/S
Having started operations in 1996, we have two decades of experience sustaining relationships with l...
Having started operations in 1996, we have two decades of experience sustaining relationships with large pharma companies by delivering quality sterile products for the Indian market. We are a company that specializes in Sterile Injectables. Our manufacturing facility has USFDA and EU GMP approvals. We manufacture sterile solutions in vials and ampoules and will have lyophilization capability by March 2021. Right from inception, we have built a reputation as a reliable supplier and partner for sterile injectables Contract Manufacturing.
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NAFDAC
Having started operations in 1996, we have two decades of experience sustaining relationships with l...
Having started operations in 1996, we have two decades of experience sustaining relationships with large pharma companies by delivering quality sterile products for the Indian market. We are a company that specializes in Sterile Injectables. Our manufacturing facility has USFDA and EU GMP approvals. We manufacture sterile solutions in vials and ampoules and will have lyophilization capability by March 2021. Right from inception, we have built a reputation as a reliable supplier and partner for sterile injectables Contract Manufacturing.
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TGA- Australia
Established in 2000, Shodhana Laboratories offers a wide range of APIs and intermediates and caters ...
Established in 2000, Shodhana Laboratories offers a wide range of APIs and intermediates and caters to the generic and custom requirements of some of the most prestigious pharma companies. It is WHO-GMP, ISO 9001-2008 and ISO 14000:2004 certified. Shodhana develops quality products through cutting-edge research, expertise and the best drug manufacturing practices. Its manufacturing processes are as per ICH guidelines and cGMP-compliant. Shodhana also has a world-class R&D lab manned by a team of highly qualified scientists. Shodhana exports the highest-quality APIs and intermediates to markets across several countries.
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Cofepris Certificate
Established in 2000, Shodhana Laboratories offers a wide range of APIs and intermediates and caters ...
Established in 2000, Shodhana Laboratories offers a wide range of APIs and intermediates and caters to the generic and custom requirements of some of the most prestigious pharma companies. It is WHO-GMP, ISO 9001-2008 and ISO 14000:2004 certified. Shodhana develops quality products through cutting-edge research, expertise and the best drug manufacturing practices. Its manufacturing processes are as per ICH guidelines and cGMP-compliant. Shodhana also has a world-class R&D lab manned by a team of highly qualified scientists. Shodhana exports the highest-quality APIs and intermediates to markets across several countries.
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INVIMA-Colombia
Founded in 1972, Eurofarma is one of the largest pharmaceutical industries in Brazil. With 100% nati...
Founded in 1972, Eurofarma is one of the largest pharmaceutical industries in Brazil. With 100% national capital, it is proud to be the first pharmaceutical multinational in Brazil. It is present in more than 20 countries and covers 87% of the Latin American market. Elected one of the 20 most innovative companies in Brazil, it launched the first biosimilar medicine in Latin America in 2016. The company is the only bi-champion pharmaceutical company by the Exame de Sustentabilidade Guide.
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DIGEMID-Peru
Founded in 1972, Eurofarma is one of the largest pharmaceutical industries in Brazil. With 100% nati...
Founded in 1972, Eurofarma is one of the largest pharmaceutical industries in Brazil. With 100% national capital, it is proud to be the first pharmaceutical multinational in Brazil. It is present in more than 20 countries and covers 87% of the Latin American market. Elected one of the 20 most innovative companies in Brazil, it launched the first biosimilar medicine in Latin America in 2016. The company is the only bi-champion pharmaceutical company by the Exame de Sustentabilidade Guide.
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GMP ANVISA- Brazil
Founded in 1972, Eurofarma is one of the largest pharmaceutical industries in Brazil. With 100% nati...
Founded in 1972, Eurofarma is one of the largest pharmaceutical industries in Brazil. With 100% national capital, it is proud to be the first pharmaceutical multinational in Brazil. It is present in more than 20 countries and covers 87% of the Latin American market. Elected one of the 20 most innovative companies in Brazil, it launched the first biosimilar medicine in Latin America in 2016. The company is the only bi-champion pharmaceutical company by the Exame de Sustentabilidade Guide.
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ANMAT-Argentina
Founded in 1972, Eurofarma is one of the largest pharmaceutical industries in Brazil. With 100% nati...
Founded in 1972, Eurofarma is one of the largest pharmaceutical industries in Brazil. With 100% national capital, it is proud to be the first pharmaceutical multinational in Brazil. It is present in more than 20 countries and covers 87% of the Latin American market. Elected one of the 20 most innovative companies in Brazil, it launched the first biosimilar medicine in Latin America in 2016. The company is the only bi-champion pharmaceutical company by the Exame de Sustentabilidade Guide.
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Kosher certified
Bio-gen Extracts Pvt. Ltd., India, established in the year 2000, is a GMP Certified fine chemicals c...
Bio-gen Extracts Pvt. Ltd., India, established in the year 2000, is a GMP Certified fine chemicals company that specializes in the process development and manufacture of Active Pharmaceutical Ingredients, Therapeutic Enzymes, Specialty Polymers & Nutraceutical Raw Materials.
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HACCP Certified
Bio-gen Extracts Pvt. Ltd., India, established in the year 2000, is a GMP Certified fine chemicals c...
Bio-gen Extracts Pvt. Ltd., India, established in the year 2000, is a GMP Certified fine chemicals company that specializes in the process development and manufacture of Active Pharmaceutical Ingredients, Therapeutic Enzymes, Specialty Polymers & Nutraceutical Raw Materials.
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ISO Certified
Bio-gen Extracts Pvt. Ltd., India, established in the year 2000, is a GMP Certified fine chemicals c...
Bio-gen Extracts Pvt. Ltd., India, established in the year 2000, is a GMP Certified fine chemicals company that specializes in the process development and manufacture of Active Pharmaceutical Ingredients, Therapeutic Enzymes, Specialty Polymers & Nutraceutical Raw Materials.
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EU GMP
WORLD MEDICINE develops and manufactures pharmaceuticals from various therapetic areas by its wholly...
WORLD MEDICINE develops and manufactures pharmaceuticals from various therapetic areas by its wholly owned factor with dosage forms including tabets (film-coated, enteric-coated), capsules (soft and hard gelatin), sachets, liquid forms (dry powder for suspension, oral solutions, syrups, granules), nasal spray, (ear and eye) drops, inhalation aerosol and micro-dose capsule anti-asthmatics.We proudly mention the contemporary R&D laboratory is one of the best. Since production is in strict conformity with USA, European standarts, they are certified by the related institutions.
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GMP
WORLD MEDICINE develops and manufactures pharmaceuticals from various therapetic areas by its wholly...
WORLD MEDICINE develops and manufactures pharmaceuticals from various therapetic areas by its wholly owned factor with dosage forms including tabets (film-coated, enteric-coated), capsules (soft and hard gelatin), sachets, liquid forms (dry powder for suspension, oral solutions, syrups, granules), nasal spray, (ear and eye) drops, inhalation aerosol and micro-dose capsule anti-asthmatics.We proudly mention the contemporary R&D laboratory is one of the best. Since production is in strict conformity with USA, European standarts, they are certified by the related institutions.
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Health Canada-GMP Foreign Compliant
RAFARM is a Greek company engaged in the development, manufacturing, in/out licensing and marketing ...
RAFARM is a Greek company engaged in the development, manufacturing, in/out licensing and marketing of pharmaceutical and OTC products. We employ 300 professionals, all experienced in their respective field. Our ISO14001 compliant and GMP approved facilities, produce solids, semisolids, liquids, creams and sterile products (injectable, ophthalmic). Our R&D team consists of highly educated experts who generate a flow of registration dossiers, leading to MAs worldwide. Domestic promotion is performed by our 85 representatives, providing nationwide coverage. We offer flexible, reliable manufacturing, several generic CTD dossiers, efficient sales force and proven ability to fulfil our customers' needs.
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Health Canada: Inspection Start Date: 2014-04-09; Type- GMP Foreign
Angelini Fine Chemicals is Angelini Pharma S.p.A. Business Unit fully dedicated to the development a...
Angelini Fine Chemicals is Angelini Pharma S.p.A. Business Unit fully dedicated to the development and manufacture of small molecules API for the global Pharmaceutical market. Angelini Fine Chemicals is a major EU CDMO serving the pharmaceutical industry. Equipped with state-of-the-art R&D labs and over 70.000 m2 cGMP manufacturing facility, Angelini Fine Chemicals is well positioned for the development and manufacturing of target molecules of relevance to the pharmaceutical market. We have a wide reaction portfolio and niche chemical technologies (such as Flow Chemistry & HPAPI) ensuring to resolve complex process chemistry & scale up issue
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Canadian GMP
Established in 2010, Pharmactive knows full well "Happy is the one who offers a cure." Pharmactive's...
Established in 2010, Pharmactive knows full well "Happy is the one who offers a cure." Pharmactive's experienced team offers drugs developed with an innovative, high quality and patient-oriented approach in various therapeutic fields for doctors, pharmacists and patients. It is one of the few leading drug production facilities both in Turkey and Europe thanks to an investment worth $200 million. Pharmactive's GMP-certified factory located in Çerkezköy on an area of 108,000 square meters boasts a production capacity of 330 million boxes of pharmaceuticals in liquid, semi-solid and solid forms.
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USFDA
Established in 1991, SM Biomed is a joint venture company pioneering the manufacture of API (active ...
Established in 1991, SM Biomed is a joint venture company pioneering the manufacture of API (active pharmaceutical ingredients) products in Malaysia. Company has grown several folds as a market leader in the manufacture of macrolide antibiotics. Quality in the products & excellent service to our clients has been the essence of our success. Asia’s largest producer and exporter of Synthetic Macrolide antibiotics.Malaysia’s largest exporter of pharmaceuticals. We shall learn, we shall seek, attain higher peaks, soar and grow as a major force for the millennium.
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TGA AUSTRALIA
Established in 1991, SM Biomed is a joint venture company pioneering the manufacture of API (active ...
Established in 1991, SM Biomed is a joint venture company pioneering the manufacture of API (active pharmaceutical ingredients) products in Malaysia. Company has grown several folds as a market leader in the manufacture of macrolide antibiotics. Quality in the products & excellent service to our clients has been the essence of our success. Asia’s largest producer and exporter of Synthetic Macrolide antibiotics.Malaysia’s largest exporter of pharmaceuticals. We shall learn, we shall seek, attain higher peaks, soar and grow as a major force for the millennium.
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EUGMP: MOH GERMANY
Established in 1991, SM Biomed is a joint venture company pioneering the manufacture of API (active ...
Established in 1991, SM Biomed is a joint venture company pioneering the manufacture of API (active pharmaceutical ingredients) products in Malaysia. Company has grown several folds as a market leader in the manufacture of macrolide antibiotics. Quality in the products & excellent service to our clients has been the essence of our success. Asia’s largest producer and exporter of Synthetic Macrolide antibiotics.Malaysia’s largest exporter of pharmaceuticals. We shall learn, we shall seek, attain higher peaks, soar and grow as a major force for the millennium.
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KFDA
Established in 1991, SM Biomed is a joint venture company pioneering the manufacture of API (active ...
Established in 1991, SM Biomed is a joint venture company pioneering the manufacture of API (active pharmaceutical ingredients) products in Malaysia. Company has grown several folds as a market leader in the manufacture of macrolide antibiotics. Quality in the products & excellent service to our clients has been the essence of our success. Asia’s largest producer and exporter of Synthetic Macrolide antibiotics.Malaysia’s largest exporter of pharmaceuticals. We shall learn, we shall seek, attain higher peaks, soar and grow as a major force for the millennium.
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GMP- Andhra Pradesh
HIRANYA CELLULOSE PRODUCTS is a manufacturer of sodium CMC,Carmellolose(Cross Linked CMC),Calcium CM...
HIRANYA CELLULOSE PRODUCTS is a manufacturer of sodium CMC,Carmellolose(Cross Linked CMC),Calcium CMC,Micro Crystalline Cellulose powder(MCCP) all grades,Colloidal grades and Sodium Starch glycolate(SSG). HCP Started in the year 2000, the company is continuously rising on the growth chart and setting very high quality standards. Our strict emphasis on quality is combined with the latest technology to offer our customers a competitive edge. Since its inception, the company has established a reputation for itself as a supplier of quality products. We focus on quality and aim to achieve total customer satisfaction, both in the products we offer and in the service that follows.
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TGA, Australia
Apothecon Pharmaceuticals is a developer & manufacturer of niche generic APIs & FDFs. It is the Indi...
Apothecon Pharmaceuticals is a developer & manufacturer of niche generic APIs & FDFs. It is the Indian counterpart of Navinta LLC, USA. Certified by all the top regulatory authorities namely-US FDA, UK MHRA, WHO & State GMP, TGA, ANVISA, MFDS & the MOH of Turkey, Russia, Libya & Yemen. With the implementation of backward integration for its product manufacturing, they have strong controls over quality & supply chain which facilitates timely deliverables. More than 15+ DMFs & ANDA filings are often amongst the first few generics in the world with their pick of complex & lucrative molecules whose development they have expertise in.
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ANVISA, Brazil
Apothecon Pharmaceuticals is a developer & manufacturer of niche generic APIs & FDFs. It is the Indi...
Apothecon Pharmaceuticals is a developer & manufacturer of niche generic APIs & FDFs. It is the Indian counterpart of Navinta LLC, USA. Certified by all the top regulatory authorities namely-US FDA, UK MHRA, WHO & State GMP, TGA, ANVISA, MFDS & the MOH of Turkey, Russia, Libya & Yemen. With the implementation of backward integration for its product manufacturing, they have strong controls over quality & supply chain which facilitates timely deliverables. More than 15+ DMFs & ANDA filings are often amongst the first few generics in the world with their pick of complex & lucrative molecules whose development they have expertise in.
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WHO-GMP
Enaltec Labs was established in 2006 by a group of young & experienced professionals with the specif...
Enaltec Labs was established in 2006 by a group of young & experienced professionals with the specific objective to develop & produce complex, small volume, technology driven products at competitive prices, thus providing the critical India advantage to generic formulators across the world. The paradigm shift of leading Indian pharmaceutical companies to target high volume and blockbuster products for regulated markets has been the inspiration behind the launch of Enaltec Labs.
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GMP
In our office in Venlo (Netherlands), we produce metal soaps, alkali soaps and dispersions.
These ...
In our office in Venlo (Netherlands), we produce metal soaps, alkali soaps and dispersions.
These products are based solely on selected, high quality vegetable fatty acids.

For many years now, Peter Greven has aligned the Venlo location consistently to the needs of the pharmaceutical, food, feed and cosmetic industry: all the products are manufactured under GMP conditions and in accordance with HACCP standards, are Kosher and Halal certified, meet all major pharmacopoeia (eg Ph. Eur, USP / NF, BP, JP, CP, DAB), the FDA guidelines for direct food contact (GRAS) and are compliant with the latest Food Chemical Codex (FCC).
In addition, a management system for food safety was introduced, which was awarded the FSSC 22000 (ISO 22000) certificate
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Kosher and Halal
In our office in Venlo (Netherlands), we produce metal soaps, alkali soaps and dispersions.
These ...
In our office in Venlo (Netherlands), we produce metal soaps, alkali soaps and dispersions.
These products are based solely on selected, high quality vegetable fatty acids.

For many years now, Peter Greven has aligned the Venlo location consistently to the needs of the pharmaceutical, food, feed and cosmetic industry: all the products are manufactured under GMP conditions and in accordance with HACCP standards, are Kosher and Halal certified, meet all major pharmacopoeia (eg Ph. Eur, USP / NF, BP, JP, CP, DAB), the FDA guidelines for direct food contact (GRAS) and are compliant with the latest Food Chemical Codex (FCC).
In addition, a management system for food safety was introduced, which was awarded the FSSC 22000 (ISO 22000) certificate
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Health Canada: Inspection Start Date: 06-05-2023; Rating- Compliant; Type of Inspection- GMP Foreign...
Health Canada: Inspection Start Date: 06-05-2023; Rating- Compliant; Type of Inspection- GMP Foreign-Regular On-Site Inspection
Curia is a global contract research, development and manufacturing organization (CDMO), offering pro...
Curia is a global contract research, development and manufacturing organization (CDMO), offering products and services across the drug development spectrum to help our partners turn their ideas into real-world impact. We partner closely with pharmaceutical and biotechnology companies to boost business performance and improve patients’ lives. From early discovery and development through manufacturing and commercialization, our suite of custom solutions allows us to tailor every engagement to your precise needs, whether that’s an independent project or an opportunity that cuts across the drug continuum.
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WHO-GMP
Anuh Pharma Ltd belong to SK group based in India. We are leading manufacturers of API'S mainly Eryt...
Anuh Pharma Ltd belong to SK group based in India. We are leading manufacturers of API'S mainly Erythromycin Salts, Azithromycin, Clarithromycin, Roxithromycin, Pyrazinamide, Chloramphenicol and various Corticosteroids like Betamethasone Salts, Dexamethasone salts, Deflazacort, Mometasone Furoate, Prednisolone Sodium Phosphate. Manufacturing facility is located in Boisar 120 km from Mumbai, Our facility is GMP approved & inspected & approved by EDQM. We have CEP & EU GMP certificate for Erythromycin, Erythromycin Ethyl Succinate & Pyrazinamide. WHO Geneva prequalifaction for Pyrazinamide. DMFS Available. We have state of art in house R&D facility located in Navi Mumbai & are open for Contract research opportunity.
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AIFA- GMP
ICROM is specialized in the manufacturing and contract manufacturing of Active Pharmaceutical Ingred...
ICROM is specialized in the manufacturing and contract manufacturing of Active Pharmaceutical Ingredients (APIs) and GMP intermediates. ICROM is the partner of choice for pharmaceutical outsourcing. Since 1969, ICROM is specialized in the manufacturing and contract manufacturing of Active Pharmaceutical Ingredients (APIs) and GMP intermediates. Thanks to the extensive experience and strong know-how, ICROM is the ideal partner for designing and tailoring projects upon customers’ needs.
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WHO-GMP Certificate- DCD/SPL-CL-1/CR-1033/2015-16
VPL Chemicals Pvt Ltd engaged in the manufacturing and exporting of various herbal/botanical extract...
VPL Chemicals Pvt Ltd engaged in the manufacturing and exporting of various herbal/botanical extracts, phytochemicals used in health supplements/ herbal medicine. VPL’s whole team is committed to deliver heighest quality products conforming international quality standards. Our strong logistic support further enables us to deliver our consignments on time to the desired destination. R & D department is equipped with state of art facility with advanced equipments backed with highly experienced research team, which has been dedicated for continual improvement in know how process while producing quality products.
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GMP- Karnataka, India
Stellence Pharmscience Private Limited is a company keenly involved in the business of manufacturing...
Stellence Pharmscience Private Limited is a company keenly involved in the business of manufacturing Active Pharmaceuticals Ingredients (API), High End Intermediates (HEIN) and Contrast Media Products (CMP). In its aspiration to locate a suitable manufacturing location in Bangalore, the company identified and acquired Karnataka Chemsyn Limited (KCL), which was under rehabilitation with the Bureau of Industrial Finance and Reconstruction (BIFR), Govt. of India. With infusion of capital into the company, it has now been rehabilitated and restructured and is a vibrant manufacturing facility located at Jigani, in South Bangalore.
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GMP- SFDA
CAD Middle East Pharmaceutical Industries LLC is a state-of-art manufacturing facility using latest ...
CAD Middle East Pharmaceutical Industries LLC is a state-of-art manufacturing facility using latest technologies with dedication to manufacture the highest quality of Active Pharmaceutical Ingredients (APIs) following current Good Manufacturing Practices (cGMP) standards. CAD Middle East Pharmaceutical Industries LLC established in Riyadh, Kingdom of Saudi Arabia. CAD manufacturing activities started in 2013. It is our guiding principle to introduce, through continuous research and development, consistent high quality following the latest GMP standards, low cost manufacturing of Innovative APIs for our diverse client base. We accomplish this by working in partnership with the clients/partners in understanding their current and future needs.
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GMP-Karnataka, India
Trimax Bio Sciences Pvt. Ltd. has been Conceived to Manufacture Pharmaceutical Intermediates and Act...
Trimax Bio Sciences Pvt. Ltd. has been Conceived to Manufacture Pharmaceutical Intermediates and Active Pharmaceutical Ingredients with Production Capacity about 400 tons per Annum with a Capital Cost of Rs.60 Crores at Raichur Industrial Estate. R&D is the Foundation of our Success in Bringing New Products to Market. Highly-Skilled Scientists are Part of our Team and they Work Towards the Discovery, Design of Novel & Effective Pharmaceutical Agents, Processes and Technologies.And so, we Wish to be a Leading Pharmaceutical Company in Healthcare.
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Drug Mfg. Licence
Trimax Bio Sciences Pvt. Ltd. has been Conceived to Manufacture Pharmaceutical Intermediates and Act...
Trimax Bio Sciences Pvt. Ltd. has been Conceived to Manufacture Pharmaceutical Intermediates and Active Pharmaceutical Ingredients with Production Capacity about 400 tons per Annum with a Capital Cost of Rs.60 Crores at Raichur Industrial Estate. R&D is the Foundation of our Success in Bringing New Products to Market. Highly-Skilled Scientists are Part of our Team and they Work Towards the Discovery, Design of Novel & Effective Pharmaceutical Agents, Processes and Technologies.And so, we Wish to be a Leading Pharmaceutical Company in Healthcare.
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ISO 9001: 2008
CurTec has close ties with the pharmaceutical industry. Ever since the first pharma company decided ...
CurTec has close ties with the pharmaceutical industry. Ever since the first pharma company decided to use our plastic drums to ship their high-value products, it has been our challenge to provide the best possible packaging solution and first class service to the industry. And that strategy paid off. Today CurTec drums and containers can be found in almost every pharmaceutical warehouse in the world. Whether acquired directly or via delivery from other pharma companies, many pharmaceutical manufacturers rely on the safety and security provided by our packaging products. CurTec adds value to the supply chain of companies producing active ingredients, excipients and solid dosage forms such as tablets and capsules. We not only supply off-the-shelf packaging but have also been asked on numerous occasions to custom design packaging solutions. Sustainable solutions that increase your customer’s satisfaction and allow cost reduction. CurTec manufactures high performance plastic packaging for pharmaceutical and chemical applications. We fulfil packaging needs of pharmaceutical companies producing active ingredients, excipients and solid dosage forms such as tablets and capsules. Adding value to your supply chain through clever packaging solutions is our target.Added value lies predominantly in the areas of cleanliness, safety and reliability. Our drums and containers are clean, safe and certified. They help you reduce supply chain cost, increase your profit and raise your customer's satisfaction.
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ISO 14001: 2004
CurTec has close ties with the pharmaceutical industry. Ever since the first pharma company decided ...
CurTec has close ties with the pharmaceutical industry. Ever since the first pharma company decided to use our plastic drums to ship their high-value products, it has been our challenge to provide the best possible packaging solution and first class service to the industry. And that strategy paid off. Today CurTec drums and containers can be found in almost every pharmaceutical warehouse in the world. Whether acquired directly or via delivery from other pharma companies, many pharmaceutical manufacturers rely on the safety and security provided by our packaging products. CurTec adds value to the supply chain of companies producing active ingredients, excipients and solid dosage forms such as tablets and capsules. We not only supply off-the-shelf packaging but have also been asked on numerous occasions to custom design packaging solutions. Sustainable solutions that increase your customer’s satisfaction and allow cost reduction. CurTec manufactures high performance plastic packaging for pharmaceutical and chemical applications. We fulfil packaging needs of pharmaceutical companies producing active ingredients, excipients and solid dosage forms such as tablets and capsules. Adding value to your supply chain through clever packaging solutions is our target.Added value lies predominantly in the areas of cleanliness, safety and reliability. Our drums and containers are clean, safe and certified. They help you reduce supply chain cost, increase your profit and raise your customer's satisfaction.
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ISO 15378: 2015
CurTec has close ties with the pharmaceutical industry. Ever since the first pharma company decided ...
CurTec has close ties with the pharmaceutical industry. Ever since the first pharma company decided to use our plastic drums to ship their high-value products, it has been our challenge to provide the best possible packaging solution and first class service to the industry. And that strategy paid off. Today CurTec drums and containers can be found in almost every pharmaceutical warehouse in the world. Whether acquired directly or via delivery from other pharma companies, many pharmaceutical manufacturers rely on the safety and security provided by our packaging products. CurTec adds value to the supply chain of companies producing active ingredients, excipients and solid dosage forms such as tablets and capsules. We not only supply off-the-shelf packaging but have also been asked on numerous occasions to custom design packaging solutions. Sustainable solutions that increase your customer’s satisfaction and allow cost reduction. CurTec manufactures high performance plastic packaging for pharmaceutical and chemical applications. We fulfil packaging needs of pharmaceutical companies producing active ingredients, excipients and solid dosage forms such as tablets and capsules. Adding value to your supply chain through clever packaging solutions is our target.Added value lies predominantly in the areas of cleanliness, safety and reliability. Our drums and containers are clean, safe and certified. They help you reduce supply chain cost, increase your profit and raise your customer's satisfaction.
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FSSC 22000
CurTec has close ties with the pharmaceutical industry. Ever since the first pharma company decided ...
CurTec has close ties with the pharmaceutical industry. Ever since the first pharma company decided to use our plastic drums to ship their high-value products, it has been our challenge to provide the best possible packaging solution and first class service to the industry. And that strategy paid off. Today CurTec drums and containers can be found in almost every pharmaceutical warehouse in the world. Whether acquired directly or via delivery from other pharma companies, many pharmaceutical manufacturers rely on the safety and security provided by our packaging products. CurTec adds value to the supply chain of companies producing active ingredients, excipients and solid dosage forms such as tablets and capsules. We not only supply off-the-shelf packaging but have also been asked on numerous occasions to custom design packaging solutions. Sustainable solutions that increase your customer’s satisfaction and allow cost reduction. CurTec manufactures high performance plastic packaging for pharmaceutical and chemical applications. We fulfil packaging needs of pharmaceutical companies producing active ingredients, excipients and solid dosage forms such as tablets and capsules. Adding value to your supply chain through clever packaging solutions is our target.Added value lies predominantly in the areas of cleanliness, safety and reliability. Our drums and containers are clean, safe and certified. They help you reduce supply chain cost, increase your profit and raise your customer's satisfaction.
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GMP
Our company, founded in 1948, and pioneered the production of capsicum and menthol plasters, thermal...
Our company, founded in 1948, and pioneered the production of capsicum and menthol plasters, thermal plasters, callus plasters, pomades and liniments which have non equipollents in our country.
The company suspended its medicine production at the end of 2001 in order to concentrate on patch and plaster production for pain relief such as Sanli Capsicum Perforated Plaster, Sanli Menthol Plaster, K. Panter Plaster and Red Pepper Perforated Plaster.
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ISO Certified
Kangcare is a bio-science technology based company in the global market with a team of specialists, ...
Kangcare is a bio-science technology based company in the global market with a team of specialists, who focuses on developing and marketing innovative and proven bioactive ingredients, and delivering science-based health and beauty solutions to customers. We always provide follow-up service, technical support and innovation suggestions, to meet customers’ demands and help them to be successful.
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FMHACA- Ethiopia
We are a fast growing Indian Pharmaceutical & Nutraceutical manufacturing company, working relentles...
We are a fast growing Indian Pharmaceutical & Nutraceutical manufacturing company, working relentlessly towards our goal of providing world class quality medicines at affordable prices.We manufacture a wide range of prescription drugs and over the counter medications. In addition, our offerings also include dietary supplements and phyto-pharmaceuticals.With a large portfolio of over 500 molecules in tablets, capsules (soft & hard gelatin), oral liquids and sachets in over 45 therapeutic classes, XL has the capacity to cater to your every need.Our offering extends across Anti-Infective, Cardiovascular, Pain Management, Gastrointestinal, Central Nervous System (CNS), and Respiratory, Anti-Fungal, Orthopedics, Nutritionals, Urology and many more.We are definitely “Your Partner on the Path of making a Healthier Mankind.”
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PIC/S (SAUMP- Ukraine)
We are a fast growing Indian Pharmaceutical & Nutraceutical manufacturing company, working relentles...
We are a fast growing Indian Pharmaceutical & Nutraceutical manufacturing company, working relentlessly towards our goal of providing world class quality medicines at affordable prices.We manufacture a wide range of prescription drugs and over the counter medications. In addition, our offerings also include dietary supplements and phyto-pharmaceuticals.With a large portfolio of over 500 molecules in tablets, capsules (soft & hard gelatin), oral liquids and sachets in over 45 therapeutic classes, XL has the capacity to cater to your every need.Our offering extends across Anti-Infective, Cardiovascular, Pain Management, Gastrointestinal, Central Nervous System (CNS), and Respiratory, Anti-Fungal, Orthopedics, Nutritionals, Urology and many more.We are definitely “Your Partner on the Path of making a Healthier Mankind.”
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EU GMP
We are a fast growing Indian Pharmaceutical & Nutraceutical manufacturing company, working relentles...
We are a fast growing Indian Pharmaceutical & Nutraceutical manufacturing company, working relentlessly towards our goal of providing world class quality medicines at affordable prices.We manufacture a wide range of prescription drugs and over the counter medications. In addition, our offerings also include dietary supplements and phyto-pharmaceuticals.With a large portfolio of over 500 molecules in tablets, capsules (soft & hard gelatin), oral liquids and sachets in over 45 therapeutic classes, XL has the capacity to cater to your every need.Our offering extends across Anti-Infective, Cardiovascular, Pain Management, Gastrointestinal, Central Nervous System (CNS), and Respiratory, Anti-Fungal, Orthopedics, Nutritionals, Urology and many more.We are definitely “Your Partner on the Path of making a Healthier Mankind.”
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GMP-Cerificate
Changzhou Pharmaceutical Factory (CPF) is a subsidiary company of Shanghai Pharma Holdings Co., Ltd....
Changzhou Pharmaceutical Factory (CPF) is a subsidiary company of Shanghai Pharma Holdings Co., Ltd., It is headquartered in Changzhou, Jiangsu Province, China. The company was founded in 1949 by (Tan Ruiting) with a registered capital of 108 million yuan and the company was restructured as a Changzhou pharmaceutical Factory under the aegis of the Shanghai Pharma Group. The company mainly involves leading pharmaceutical manufacturers a wide range of key Intermediates, Active pharmaceutical ingredients, and Finished Formulations that meet with global standards.
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AIFA- Italy
Lusochimica S.p.A. is an Italian manufacturer of bulk active ingredients for pharmaceuticals (API), ...
Lusochimica S.p.A. is an Italian manufacturer of bulk active ingredients for pharmaceuticals (API), having sales offices in Milan and two production plants in Lomagna and Pisa, whose production processes strictly comply with international cGMP standards. Founded in 1964 and belonging to Menarini Group since 1984, Lusochimica S.p.A. incorporated former Laboratori Guidotti Fine Chemicals division starting January 2009, as a result of restructuring of Fine Chemicals operations within Menarini Group. Lusochimica’s mission is to dedicate our cutting edge manufacturing technology to ensure supplying high quality active ingredients to our clients because, according to our vision, safety of human drugs must be the driving force of our daily actions.
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AIFA- Italy
Lusochimica S.p.A. is an Italian manufacturer of bulk active ingredients for pharmaceuticals (API), ...
Lusochimica S.p.A. is an Italian manufacturer of bulk active ingredients for pharmaceuticals (API), having sales offices in Milan and two production plants in Lomagna and Pisa, whose production processes strictly comply with international cGMP standards. Founded in 1964 and belonging to Menarini Group since 1984, Lusochimica S.p.A. incorporated former Laboratori Guidotti Fine Chemicals division starting January 2009, as a result of restructuring of Fine Chemicals operations within Menarini Group. Lusochimica’s mission is to dedicate our cutting edge manufacturing technology to ensure supplying high quality active ingredients to our clients because, according to our vision, safety of human drugs must be the driving force of our daily actions.
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OTHERS
Laurus Labs is a leading research and development-driven pharmaceutical company in India. The compan...
Laurus Labs is a leading research and development-driven pharmaceutical company in India. The company has grown consistently to become one of the leading manufacturers of Active Pharmaceutical Ingredients (APIs) for anti-retroviral (ARV) and Hepatitis C. Laurus Labs also manufactures APIs in oncology and other therapeutic areas. Its strategic and early investments in R&D and manufacturing infrastructure have enabled it to become one of the leading suppliers of APIs in the ARV therapeutic area. Out of Ten largest generic pharmaceutical companies in the world, by revenues, are our customers.
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TGA - Australia
Titan Laboratories is leading EU GMP approved Site for Sustained and Modified Release Pellets, Direc...
Titan Laboratories is leading EU GMP approved Site for Sustained and Modified Release Pellets, Direct Compressible Granules, Tablets & Capsules.Our major focus in EU market is for1) CONTRACT MANUFACTURING SERVICES:-> As approved Dossier Manufacturer.-> Site variation basis.-> cGMP pilot batch for BE/BA or Clinical Studies.2) CONTRACT RESEARCH SERVICES:-> Product Development - Generic Equivalent, Novel Sustained & Combination Products-> Method Development & Validation-> Dossier Preparation-> Stability Studies
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Korea - MFDS
Titan Laboratories is leading EU GMP approved Site for Sustained and Modified Release Pellets, Direc...
Titan Laboratories is leading EU GMP approved Site for Sustained and Modified Release Pellets, Direct Compressible Granules, Tablets & Capsules.Our major focus in EU market is for1) CONTRACT MANUFACTURING SERVICES:-> As approved Dossier Manufacturer.-> Site variation basis.-> cGMP pilot batch for BE/BA or Clinical Studies.2) CONTRACT RESEARCH SERVICES:-> Product Development - Generic Equivalent, Novel Sustained & Combination Products-> Method Development & Validation-> Dossier Preparation-> Stability Studies
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Colombia - Invima
Titan Laboratories is leading EU GMP approved Site for Sustained and Modified Release Pellets, Direc...
Titan Laboratories is leading EU GMP approved Site for Sustained and Modified Release Pellets, Direct Compressible Granules, Tablets & Capsules.Our major focus in EU market is for1) CONTRACT MANUFACTURING SERVICES:-> As approved Dossier Manufacturer.-> Site variation basis.-> cGMP pilot batch for BE/BA or Clinical Studies.2) CONTRACT RESEARCH SERVICES:-> Product Development - Generic Equivalent, Novel Sustained & Combination Products-> Method Development & Validation-> Dossier Preparation-> Stability Studies
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Ethiopian - GMP
Titan Laboratories is leading EU GMP approved Site for Sustained and Modified Release Pellets, Direc...
Titan Laboratories is leading EU GMP approved Site for Sustained and Modified Release Pellets, Direct Compressible Granules, Tablets & Capsules.Our major focus in EU market is for1) CONTRACT MANUFACTURING SERVICES:-> As approved Dossier Manufacturer.-> Site variation basis.-> cGMP pilot batch for BE/BA or Clinical Studies.2) CONTRACT RESEARCH SERVICES:-> Product Development - Generic Equivalent, Novel Sustained & Combination Products-> Method Development & Validation-> Dossier Preparation-> Stability Studies
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GMP Certified
Founded in 2002, JQC (Huayin) Pharmaceutical Co., Ltd. is a private pharmaceutical enterprise, that ...
Founded in 2002, JQC (Huayin) Pharmaceutical Co., Ltd. is a private pharmaceutical enterprise, that focus in Salicylic acid series API & intermediates production and research development. The predecessor was a state-owned corporation-“Northwest Second Synthesis Pharmaceutical”. The company’s register capital is 11.18 million RMB and the current net capital is nearly 150 million RMB. The company passed GMP issued by the State Food and Drug Administration (SFDA) in 2004, 2010 and 2015.Meanwhile, our quality system passed US FDA inspection In January 26, 2013, and NDC code was registered in D&B.
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GMP
Murli Krishna Pharma Private Ltd. is a young and dynamic drug delivery systems (DDS) company in Indi...
Murli Krishna Pharma Private Ltd. is a young and dynamic drug delivery systems (DDS) company in India that provides a range of effective solutions to optimize the delivery of pharmaceutical products.
Our manufacturing plant is approved for GMP Compliance by the WHO and the European Union; Murli Krishna Pharma is equipped to undertake formulation development projects on oral NDDS.
Our encapsulation covers micro pellets & this expertise is being extended to the development of nano-particles.
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FDA- Jordan
Murli Krishna Pharma Private Ltd. is a young and dynamic drug delivery systems (DDS) company in Indi...
Murli Krishna Pharma Private Ltd. is a young and dynamic drug delivery systems (DDS) company in India that provides a range of effective solutions to optimize the delivery of pharmaceutical products.
Our manufacturing plant is approved for GMP Compliance by the WHO and the European Union; Murli Krishna Pharma is equipped to undertake formulation development projects on oral NDDS.
Our encapsulation covers micro pellets & this expertise is being extended to the development of nano-particles.
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GMP Certificate (FDA Maharashtra State)
Alkaloids is a family company established in 1967. Starting with production of natural Caffeine, qu...
Alkaloids is a family company established in 1967. Starting with production of natural Caffeine, quite a number of speciality products have been added to our portfolio. The Company is dedicated to identification, development, production & distribution of potent Phytochemicals and Botanical extracts. A number of Phytochemicals manufactured by Alkaloids are used as Active Pharmaceutical Ingredients by major drug formulators the world over. We are internationally recognised as a reliable supplier of high quality Phyto-products. Alkaloids also manufactures custom-made products on exclusive basis for our valued customers.
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TGA Australia - GMP Certificate MI-2015-CE-00394-1
Alkaloids is a family company established in 1967. Starting with production of natural Caffeine, qu...
Alkaloids is a family company established in 1967. Starting with production of natural Caffeine, quite a number of speciality products have been added to our portfolio. The Company is dedicated to identification, development, production & distribution of potent Phytochemicals and Botanical extracts. A number of Phytochemicals manufactured by Alkaloids are used as Active Pharmaceutical Ingredients by major drug formulators the world over. We are internationally recognised as a reliable supplier of high quality Phyto-products. Alkaloids also manufactures custom-made products on exclusive basis for our valued customers.
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USFDA EIR Letter - 2018
Alkaloids is a family company established in 1967. Starting with production of natural Caffeine, qu...
Alkaloids is a family company established in 1967. Starting with production of natural Caffeine, quite a number of speciality products have been added to our portfolio. The Company is dedicated to identification, development, production & distribution of potent Phytochemicals and Botanical extracts. A number of Phytochemicals manufactured by Alkaloids are used as Active Pharmaceutical Ingredients by major drug formulators the world over. We are internationally recognised as a reliable supplier of high quality Phyto-products. Alkaloids also manufactures custom-made products on exclusive basis for our valued customers.
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W.H.O GMP
We are specialized in manufacturing of Non Pareil Seeds, Active Drug Coated (AC), Enteric Coated (EC...
We are specialized in manufacturing of Non Pareil Seeds, Active Drug Coated (AC), Enteric Coated (EC), Sustained Release (SR), Delayed Release (DR), Time Release (TR) Extended Release (ER), Controlled Release (CR) Pellets and Blended Pellets of Vitamins, anti oxidants, anti ulcerants etc. These are ready to fill pellets, making capsule manufacturing a simple, one stage process. These pellets can be directly filled in to capsules (without the hassles of drug maxing , blending etc) and sold with your own brand names. Our products are of International Standards and custom made.
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ISO 9001:2008 Certificate
We are specialized in manufacturing of Non Pareil Seeds, Active Drug Coated (AC), Enteric Coated (EC...
We are specialized in manufacturing of Non Pareil Seeds, Active Drug Coated (AC), Enteric Coated (EC), Sustained Release (SR), Delayed Release (DR), Time Release (TR) Extended Release (ER), Controlled Release (CR) Pellets and Blended Pellets of Vitamins, anti oxidants, anti ulcerants etc. These are ready to fill pellets, making capsule manufacturing a simple, one stage process. These pellets can be directly filled in to capsules (without the hassles of drug maxing , blending etc) and sold with your own brand names. Our products are of International Standards and custom made.
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WHO GMP- UQ-5731
Farbe Firma was incorporated in the year 2012. It was started as a Dyes’ and Pharmaceutical interm...
Farbe Firma was incorporated in the year 2012. It was started as a Dyes’ and Pharmaceutical intermediates trading company. We have now ventured to diversify into Injectable Pharmaceutical formulations. The company has signed an MOU (Memorandum of Understanding) with Government of Gujarat under the “Vibrant Gujarat 2015”. The company aims at providing contract manufacturing services to esteem and ambitious National and Multinational partners. At Farbe Firma “QUALITY” is being imbibed from the roots and considered as a “NECESSITY” and “EDGE” for healthy and long-lasting partnership.
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SWISS CERT-Quality Management System ISO 9001:2015
Farbe Firma was incorporated in the year 2012. It was started as a Dyes’ and Pharmaceutical interm...
Farbe Firma was incorporated in the year 2012. It was started as a Dyes’ and Pharmaceutical intermediates trading company. We have now ventured to diversify into Injectable Pharmaceutical formulations. The company has signed an MOU (Memorandum of Understanding) with Government of Gujarat under the “Vibrant Gujarat 2015”. The company aims at providing contract manufacturing services to esteem and ambitious National and Multinational partners. At Farbe Firma “QUALITY” is being imbibed from the roots and considered as a “NECESSITY” and “EDGE” for healthy and long-lasting partnership.
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GMP- Certificate No: S-GMP1706157
We are enforced with strong business ethics and unbound commitment to our clients which has enabled ...
We are enforced with strong business ethics and unbound commitment to our clients which has enabled us to achieve such heights. As we build our strategies to promote growth for the years to come, our ideas of value creation, teamwork & constant progress will continue to be the driving force of our initiatives.
Apart from our manufacturing unit where we manufacture Calamine powder (IP/BP/USP/Cosmetic grade) and Triticum Vulgare Aq. Extract, we also do contract manufacturing of Calamine lotion, Calamine prickly heat powder, Calamine cream.
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GLP- Certificate No: G/25/2204
We are enforced with strong business ethics and unbound commitment to our clients which has enabled ...
We are enforced with strong business ethics and unbound commitment to our clients which has enabled us to achieve such heights. As we build our strategies to promote growth for the years to come, our ideas of value creation, teamwork & constant progress will continue to be the driving force of our initiatives.
Apart from our manufacturing unit where we manufacture Calamine powder (IP/BP/USP/Cosmetic grade) and Triticum Vulgare Aq. Extract, we also do contract manufacturing of Calamine lotion, Calamine prickly heat powder, Calamine cream.
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ISO 9001: 2015
We are enforced with strong business ethics and unbound commitment to our clients which has enabled ...
We are enforced with strong business ethics and unbound commitment to our clients which has enabled us to achieve such heights. As we build our strategies to promote growth for the years to come, our ideas of value creation, teamwork & constant progress will continue to be the driving force of our initiatives.
Apart from our manufacturing unit where we manufacture Calamine powder (IP/BP/USP/Cosmetic grade) and Triticum Vulgare Aq. Extract, we also do contract manufacturing of Calamine lotion, Calamine prickly heat powder, Calamine cream.
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ANVISA
Unither Pharmaceuticals, international CDMO, is the worldwide leader in Sterile Unit Doses (BFS) Man...
Unither Pharmaceuticals, international CDMO, is the worldwide leader in Sterile Unit Doses (BFS) Manufacturing & offers Pharmaceutical Development & Manufacturing services for various liquid & solid dosage forms. Unither produces highly competitive niche drug products & medical devices, sterile unit-dose vials using Blow-Fill-Seal technology, preservative free multi dose for sterile products - high-barrier, single-use liquid stick packs, bottles, sprays, tablets and capsules, suppositories & ovules. We offer global or stand-alone services in drug product development, formulation, analytical development & validation, etc.
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KFDA
Unither Pharmaceuticals, international CDMO, is the worldwide leader in Sterile Unit Doses (BFS) Man...
Unither Pharmaceuticals, international CDMO, is the worldwide leader in Sterile Unit Doses (BFS) Manufacturing & offers Pharmaceutical Development & Manufacturing services for various liquid & solid dosage forms. Unither produces highly competitive niche drug products & medical devices, sterile unit-dose vials using Blow-Fill-Seal technology, preservative free multi dose for sterile products - high-barrier, single-use liquid stick packs, bottles, sprays, tablets and capsules, suppositories & ovules. We offer global or stand-alone services in drug product development, formulation, analytical development & validation, etc.
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EMEA
Unither Pharmaceuticals, international CDMO, is the worldwide leader in Sterile Unit Doses (BFS) Man...
Unither Pharmaceuticals, international CDMO, is the worldwide leader in Sterile Unit Doses (BFS) Manufacturing & offers Pharmaceutical Development & Manufacturing services for various liquid & solid dosage forms. Unither produces highly competitive niche drug products & medical devices, sterile unit-dose vials using Blow-Fill-Seal technology, preservative free multi dose for sterile products - high-barrier, single-use liquid stick packs, bottles, sprays, tablets and capsules, suppositories & ovules. We offer global or stand-alone services in drug product development, formulation, analytical development & validation, etc.
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Health Canada: Inspection Start Date: 2015-03-17; Type- GMP Foreign
Cebiphar, French CRO member of TERANGA Group, offers its expertise and technical platform to the pha...
Cebiphar, French CRO member of TERANGA Group, offers its expertise and technical platform to the pharmaceutical industry. Our key services: analytical development, stability studies, quality control (physico-chemical and microbiological), troubleshooting, technical & regulatory affairs (CMC), cleaning validation, consulting, training. Cebiphar in figures: 40 years experience, more than 2000 products being studied. GMP-compliant pharmaceutical site (ANSM & ANSES), FDA-inspected.
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Health Canada- GMP Foreign Inspection, 2015-07-09
Pierre Fabre designs, develops, produces, and markets pharmaceutical products for customers in Franc...
Pierre Fabre designs, develops, produces, and markets pharmaceutical products for customers in France and internationally. The company offers prescription drugs for various treatment fields, such as urology, gynecology, diabetes, cardiology, neuropsychiatry, rheumatology, and pneumo-allergology, as well as onco-hematology/oncology and dermatology to health care professionals and their patients. It also provides a range of prescription and over-the-counter drugs for various therapeutic areas, as well as day-to-day general health care, including oral care and natural health care to pharmacists, health care professionals, and patients.
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Health Canada- GMP Foreign Inspection, 2014-08-29
Pierre Fabre designs, develops, produces, and markets pharmaceutical products for customers in Franc...
Pierre Fabre designs, develops, produces, and markets pharmaceutical products for customers in France and internationally. The company offers prescription drugs for various treatment fields, such as urology, gynecology, diabetes, cardiology, neuropsychiatry, rheumatology, and pneumo-allergology, as well as onco-hematology/oncology and dermatology to health care professionals and their patients. It also provides a range of prescription and over-the-counter drugs for various therapeutic areas, as well as day-to-day general health care, including oral care and natural health care to pharmacists, health care professionals, and patients.
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Health Canada: Inspection Start Date: 2016-04-21 ; Type- GMP Foreign
Procos S.p.A. is a wholly owned subsidiary of the Japanese company, CBC Co. Ltd Group, specializing ...
Procos S.p.A. is a wholly owned subsidiary of the Japanese company, CBC Co. Ltd Group, specializing in the development, scale-up and production of Active Pharmaceutical Ingredients (APIs), advanced intermediates and related services for the pharmaceutical industry. Our core business sectors include custom synthesis and Generic API manufacturing. The manufacturing site is located in Cameri, Italy. This 110,000 sq. meter, cutting-edge multipurpose plant, fully designed under cGMP compliance, has been successfully audited and approved by the main regulatory authorities including AIFA, FDA and PMDA.
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Health Canada: Inspection Start Date: 2013-10-31; Type- GMP Foreign
Procos S.p.A. is a wholly owned subsidiary of the Japanese company, CBC Co. Ltd Group, specializing ...
Procos S.p.A. is a wholly owned subsidiary of the Japanese company, CBC Co. Ltd Group, specializing in the development, scale-up and production of Active Pharmaceutical Ingredients (APIs), advanced intermediates and related services for the pharmaceutical industry. Our core business sectors include custom synthesis and Generic API manufacturing. The manufacturing site is located in Cameri, Italy. This 110,000 sq. meter, cutting-edge multipurpose plant, fully designed under cGMP compliance, has been successfully audited and approved by the main regulatory authorities including AIFA, FDA and PMDA.
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GMP Certificate Number: S-GMP/1705115
Reine Lifescience is a highly acclaimed name among manufacturers and exporters of a wide variety of ...
Reine Lifescience is a highly acclaimed name among manufacturers and exporters of a wide variety of pharmaceuticals drugs.The Company Was Established in 1997 in GIDC, Ankleshwar Industry. GIDC, Ankleshwar Industry is Big Pharma and Chemical Industrial Area in Gujarat. and Reine Lifescience is one of the Highly Grossing company in Pharma and Chemical Industry.
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GLP CERTI/REINE/2017/57/871
Reine Lifescience is a highly acclaimed name among manufacturers and exporters of a wide variety of ...
Reine Lifescience is a highly acclaimed name among manufacturers and exporters of a wide variety of pharmaceuticals drugs.The Company Was Established in 1997 in GIDC, Ankleshwar Industry. GIDC, Ankleshwar Industry is Big Pharma and Chemical Industrial Area in Gujarat. and Reine Lifescience is one of the Highly Grossing company in Pharma and Chemical Industry.
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GMP Certificate; NEW-WHO-GMP/CERT/KD/62737/2018/11/22171
SAI-TECH PHARMACEUTICALS PRIVATE LIMITED is dedicated Active Pharmaceutical Ingredients (API) manufa...
SAI-TECH PHARMACEUTICALS PRIVATE LIMITED is dedicated Active Pharmaceutical Ingredients (API) manufacturing company for producing & providing high quality products as per customer requirements. We tailor molecules according to customer requirements. The company is located in Navi Mumbai in the heart of India’s Industrial Area (i.e. TTC Industrial Area) from where best possible logistic support for R & D and other business transactions will takes place.
We are ready to supply a product from gram to kilogram scale and from laboratory to pilot plant to large (commercial) scale production.
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FDA_EIR
Founded in 1995, Shenzhen Oriental Pharma focussed on the production of Active Pharma Ingredients (A...
Founded in 1995, Shenzhen Oriental Pharma focussed on the production of Active Pharma Ingredients (APIs), Now the main product is Phenylephrine Hcl (PE), Doxylamine succinate.We have 14 years production experience for Phenylephrine Hcl, granted the GMP for PE in 2004,re-certified in 2009. A DMF has been submitted to FDA in 2005 (DMF # 18799), this product passed the US FDA inspection in March 2014. According to the customer’s needs, we can supply the APIs conforming to the current standard of USP, EP and CP .At the same time, we can supply various particle sizes product.
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GMP
Founded in 1995, Shenzhen Oriental Pharma focussed on the production of Active Pharma Ingredients (A...
Founded in 1995, Shenzhen Oriental Pharma focussed on the production of Active Pharma Ingredients (APIs), Now the main product is Phenylephrine Hcl (PE), Doxylamine succinate.We have 14 years production experience for Phenylephrine Hcl, granted the GMP for PE in 2004,re-certified in 2009. A DMF has been submitted to FDA in 2005 (DMF # 18799), this product passed the US FDA inspection in March 2014. According to the customer’s needs, we can supply the APIs conforming to the current standard of USP, EP and CP .At the same time, we can supply various particle sizes product.
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GMP Inspection
Ramdev Chemicals Pvt. Ltd. is one of the fastest growing Active Pharmaceuticl Drugs, Drug Intermedia...
Ramdev Chemicals Pvt. Ltd. is one of the fastest growing Active Pharmaceuticl Drugs, Drug Intermediates, Storage Fine Chemical Company in India which have specialty in Synthesis Molecules & Chemical Preparation. We are Bulk Drugs and Chemical manufactures, Suppliers and Exporters. We have very strong team of Technocrats & Technical People engaged mainly into the New Molecules for various Multinational Companies. The company is now aimed towards the International Market & as our first step to it, we have started implementation of ISO 9001:2000 which is expected to be completed by end of 2002.
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Quality Service Certificate
Ramdev Chemicals Pvt. Ltd. is one of the fastest growing Active Pharmaceuticl Drugs, Drug Intermedia...
Ramdev Chemicals Pvt. Ltd. is one of the fastest growing Active Pharmaceuticl Drugs, Drug Intermediates, Storage Fine Chemical Company in India which have specialty in Synthesis Molecules & Chemical Preparation. We are Bulk Drugs and Chemical manufactures, Suppliers and Exporters. We have very strong team of Technocrats & Technical People engaged mainly into the New Molecules for various Multinational Companies. The company is now aimed towards the International Market & as our first step to it, we have started implementation of ISO 9001:2000 which is expected to be completed by end of 2002.
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OTHERS
ICBio is one of the leading full services CRO in Asia, based in Bangalore INDIA, engaged in conduct ...
ICBio is one of the leading full services CRO in Asia, based in Bangalore INDIA, engaged in conduct of Clinical Development and BA / BE studies Services to the Pharmaceuticals, Biotech, Nutraceuticals and Cosmetics Industries.ICBio has vast expertise in clinical trial and project management, having conducted complex clinical development programs of biologics, small molecules, and completed them within the time and cost constraints laid out by the clients. We accommodate sponsors interest in sync with lines and milestones.
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OTHERS
Jiangsu Zhongbang Pharmaceutical Co., Ltd. is a wholly-owned subsidiary of Red Sun Group. Company ha...
Jiangsu Zhongbang Pharmaceutical Co., Ltd. is a wholly-owned subsidiary of Red Sun Group. Company has been founded since 2001 and occupied 100,000m2. Company has 80 million RMB registered capital and plan to have a total investment of 200 million RMB. Company has 168 employees at present, in which there are 34 employees with Bachelor’s Degree or above, 12 employees with Master’s Degree or above, each kind of professional talents have occupied over 60% of the total employees. Company has got China GMP certificate since 2006 and currently has one GMP plant for API and one GMP plant for solid finished products. There are two production lines in API GMP plants with annual capacity of 50 tons API. There are equipment for tablets, capsules and granules in solid finished products. Company has set up qualified documentation systems according to China GMP and Europe and USA C-GMP. Company has the plan to pass COS and FDA authentication both around 2014. Company also pays serious attention on public welfare and concerns on green energy conservation and environmental protection undertaking.
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GLP Certified-NGCMA, India
Dabur Research Foundation (DRF) is an Indian Contract Research Organization offering pre-clinical se...
Dabur Research Foundation (DRF) is an Indian Contract Research Organization offering pre-clinical services in Drug Discovery and Development, ranging from identification of potential lead molecules, drug development to IND enabling studies. We offer pre-clinical services to global Biotech, Pharma, Phytopharmaceuticals Cosmescuticals and academia sectors.
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OTHERS
Instilled in the company is the DNA of complementary skills held by its founder engineer, Alberto Ma...
Instilled in the company is the DNA of complementary skills held by its founder engineer, Alberto Martinoli: the art of designing and specifying mills and, on the other hand, the art of simply raising service levels to an absolute maximum 1986: After about twenty years of experience, in response to the demand for increased globalisation and more streamlined logistics, JETPHARMA SA is born, appropriately enough in the country that was, and still remains, the industry leader. JETPHARMA SA has always aimed for excellence and maximum quality in its daily endeavour to fulfil customer requests, whether complex or not.
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OTHERS
Instilled in the company is the DNA of complementary skills held by its founder engineer, Alberto Ma...
Instilled in the company is the DNA of complementary skills held by its founder engineer, Alberto Martinoli: the art of designing and specifying mills and, on the other hand, the art of simply raising service levels to an absolute maximum 1986: After about twenty years of experience, in response to the demand for increased globalisation and more streamlined logistics, JETPHARMA SA is born, appropriately enough in the country that was, and still remains, the industry leader. JETPHARMA SA has always aimed for excellence and maximum quality in its daily endeavour to fulfil customer requests, whether complex or not.
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OTHERS
Microchem S.r.l. provides contract micronization of active and excipient ingredients for the pharmac...
Microchem S.r.l. provides contract micronization of active and excipient ingredients for the pharmaceutical industry.Our contract micronization services have been refined and improved based on actual in-depth experience gained from our daily processing operations. Our state-of-the art material handling service applies micronization technology based on this combination of improved equipment and practiced, processing skill.Microchem operates under a comprehensive Quality System to comply with all regulatory authorities and harmonized requirements. Microchem is GMP compliance and ISO Certified.
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OTHERS
Microchem S.r.l. provides contract micronization of active and excipient ingredients for the pharmac...
Microchem S.r.l. provides contract micronization of active and excipient ingredients for the pharmaceutical industry.Our contract micronization services have been refined and improved based on actual in-depth experience gained from our daily processing operations. Our state-of-the art material handling service applies micronization technology based on this combination of improved equipment and practiced, processing skill.Microchem operates under a comprehensive Quality System to comply with all regulatory authorities and harmonized requirements. Microchem is GMP compliance and ISO Certified.
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USFDA-EIR
Megsan is an emerging contract research organization (CRO) which offers analytical testing services ...
Megsan is an emerging contract research organization (CRO) which offers analytical testing services to several industries across the globe. We are an independent third party testing laboratory, not part of a company, institution or group that would impact the unbiased results we provide to our clients. We understand the need of our clients and demands of the industry, so we can handle high sample volumes, deliver the accurate results at reasonable cost with fastest turnaround time. We provide a unique tracking number upon receipt of samples, analysis requested, anticipated turnaround time to ease the process.
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ISO 9001:2015
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily include...
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily includes Oncology, Hormone, Anti-biotics and Nutraceuticals. We are a one stop smarter solution for all the Formulation like Anti Cancer Injectables, Tablets, Capsule , Syrups requirements to cope with the necessity of ailing humanity and enhancing the quality of human life. To successfully meet the growing demands of the pharmaceutical industry, Health Biotech Ltd., keeps pace with the latest technological developments, for Manufacturing finished Pharmaceutical Formulation.
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MOH Iraq
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily include...
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily includes Oncology, Hormone, Anti-biotics and Nutraceuticals. We are a one stop smarter solution for all the Formulation like Anti Cancer Injectables, Tablets, Capsule , Syrups requirements to cope with the necessity of ailing humanity and enhancing the quality of human life. To successfully meet the growing demands of the pharmaceutical industry, Health Biotech Ltd., keeps pace with the latest technological developments, for Manufacturing finished Pharmaceutical Formulation.
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MOH Syria
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily include...
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily includes Oncology, Hormone, Anti-biotics and Nutraceuticals. We are a one stop smarter solution for all the Formulation like Anti Cancer Injectables, Tablets, Capsule , Syrups requirements to cope with the necessity of ailing humanity and enhancing the quality of human life. To successfully meet the growing demands of the pharmaceutical industry, Health Biotech Ltd., keeps pace with the latest technological developments, for Manufacturing finished Pharmaceutical Formulation.
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MOH Yemen
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily include...
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily includes Oncology, Hormone, Anti-biotics and Nutraceuticals. We are a one stop smarter solution for all the Formulation like Anti Cancer Injectables, Tablets, Capsule , Syrups requirements to cope with the necessity of ailing humanity and enhancing the quality of human life. To successfully meet the growing demands of the pharmaceutical industry, Health Biotech Ltd., keeps pace with the latest technological developments, for Manufacturing finished Pharmaceutical Formulation.
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MOH Cambodia
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily include...
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily includes Oncology, Hormone, Anti-biotics and Nutraceuticals. We are a one stop smarter solution for all the Formulation like Anti Cancer Injectables, Tablets, Capsule , Syrups requirements to cope with the necessity of ailing humanity and enhancing the quality of human life. To successfully meet the growing demands of the pharmaceutical industry, Health Biotech Ltd., keeps pace with the latest technological developments, for Manufacturing finished Pharmaceutical Formulation.
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MOH Sri Lanka
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily include...
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily includes Oncology, Hormone, Anti-biotics and Nutraceuticals. We are a one stop smarter solution for all the Formulation like Anti Cancer Injectables, Tablets, Capsule , Syrups requirements to cope with the necessity of ailing humanity and enhancing the quality of human life. To successfully meet the growing demands of the pharmaceutical industry, Health Biotech Ltd., keeps pace with the latest technological developments, for Manufacturing finished Pharmaceutical Formulation.
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MOH Nigeria
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily include...
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily includes Oncology, Hormone, Anti-biotics and Nutraceuticals. We are a one stop smarter solution for all the Formulation like Anti Cancer Injectables, Tablets, Capsule , Syrups requirements to cope with the necessity of ailing humanity and enhancing the quality of human life. To successfully meet the growing demands of the pharmaceutical industry, Health Biotech Ltd., keeps pace with the latest technological developments, for Manufacturing finished Pharmaceutical Formulation.
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MOH Vietnam
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily include...
Health Biotech Ltd currently exports product in around 50 countries worldwide that primarily includes Oncology, Hormone, Anti-biotics and Nutraceuticals. We are a one stop smarter solution for all the Formulation like Anti Cancer Injectables, Tablets, Capsule , Syrups requirements to cope with the necessity of ailing humanity and enhancing the quality of human life. To successfully meet the growing demands of the pharmaceutical industry, Health Biotech Ltd., keeps pace with the latest technological developments, for Manufacturing finished Pharmaceutical Formulation.
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PMDA, KFDA & COFEPRIS
Akums Lifescience Ltd. is a research-based, vertically integrated company specializing in the develo...
Akums Lifescience Ltd. is a research-based, vertically integrated company specializing in the development, manufacturing and sale of APIs and intermediates. Akums has established itself as a leading generic medicine manufacturing company from India, with clients in over 51 countries. It has a facility dedicated to custom research and synthesis. Akums’ manufacturing facilities are spread across three locations in two Indian states. Its stringent policies and procedures ensure that that all regulatory requirements, environmental standards, and technological trends are met. Akums is EU-GMP, KFDA, WHO-GMP and PMDA certified.
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