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API SUPPLIERS
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USDMF
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Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
Certificate Number : CEP 2023-165 - Rev 00
Status : Valid
Issue Date : 2024-09-27
Type : Chemical
Substance Number : 1648
Reliable Spanish CDMO Delivering High-Quality APIs and Intermediates with Excellence, Flexibility, and Regulatory Compliance.
Certificate Number : CEP 2024-321 - Rev 00
Status : Valid
Issue Date : 2025-12-11
Type : Chemical
Substance Number : 1648
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Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2025-01-23
Registration Number : 20250123-166-I-690-20
Manufacturer Name : Tagoor Laboratories Private ...
Manufacturer Address : Unit-III,Plot No.12, JNPharma City, Parawada (mdl), Anakapalli Dist.-531021, Andhra P...
Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
Registrant Name : Pharmaline Co., Ltd.
Registration Date : 2025-06-02
Registration Number : 20250123-166-I-690-20(A)
Manufacturer Name : Tagoor Laboratories Private ...
Manufacturer Address : Unit-III,Plot No.12, JNPharma City, Parawada (mdl), Anakapalli District - 531021, And...
Reliable Spanish CDMO Delivering High-Quality APIs and Intermediates with Excellence, Flexibility, and Regulatory Compliance.
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2017-09-07
Registration Number : 20170907-166-I-526-12
Manufacturer Name : Kinsy SL
Manufacturer Address : Avda. Europa s/n, Parque Industrial de Alhama, Alhama de Murcia 30840, Spain
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Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
About the Company : Tagoor Laboratories, established in 2018 and part of the Tagoor Group, provides APIs, advanced intermediates, and key starting materials for critical and high-growth therapeutic ar...
Basic Nutrition, your expert for sourcing from China, India and Europe.
About the Company : As an ISO9001, ISO22000 certificated supplier, Basic Nutrition supply high-quality ingredients for nutraceuticals. We can offer a range of products from small to large quantites: h...
Reliable Spanish CDMO Delivering High-Quality APIs and Intermediates with Excellence, Flexibility, and Regulatory Compliance.
About the Company : Kinsy is an independent CDMO in Spain with over 30 years of experience in developing and manufacturing pharmaceutical intermediates and APIs. The company provides route development...
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
About the Company : LGM Pharma is a global leader in sourcing APIs, including hard-to-find drug substances, for pharmaceutical and biotech industries. LGM also operates as a full-service drug product ...
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
About the Company : Rochem, established in 1994, is a global distributor of pharmaceutical, food, nutritional, and animal health ingredients, sourcing high-quality products from China. Headquartered i...
Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
About the Company : Established in 1991, Pharm-Rx is an importer and distributor of active ingredients serving the pharmaceutical, nutritional supplement, and food industries. The company follows a hi...
AMI Lifesciences is Driven by Chemistry. Powered by People.
About the Company : Ami Lifesciences, established in 2006, is a rapidly growing API manufacturing company in India with strong capabilities in cardiovascular, anti-diabetic, CNS, and respiratory thera...
Willow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.
About the Company : Willow Birch Pharma, Inc. is a premier supplier of bulk APIs to North American Compounding Pharmacies, sourcing from FDA registered and GMP manufacturers. With licenses in all 50 s...
Panvo Organics: Advancing quality APIs and formulations with Halal, Kosher, US FDA, and WHO-approved manufacturing excellence.
About the Company : Panvo Organics Pvt. Ltd., established in 2006, is a WHO-GMP certified manufacturer of Active Pharmaceutical Ingredients, novel formulations, and sustainable agriculture inputs. The...
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PharmaCompass offers a list of Alpha Lipoic Acid API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Alpha Lipoic Acid manufacturer or Alpha Lipoic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Alpha Lipoic Acid manufacturer or Alpha Lipoic Acid supplier.
A BRN 0122410 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BRN 0122410, including repackagers and relabelers. The FDA regulates BRN 0122410 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BRN 0122410 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of BRN 0122410 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A BRN 0122410 supplier is an individual or a company that provides BRN 0122410 active pharmaceutical ingredient (API) or BRN 0122410 finished formulations upon request. The BRN 0122410 suppliers may include BRN 0122410 API manufacturers, exporters, distributors and traders.
click here to find a list of BRN 0122410 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A BRN 0122410 DMF (Drug Master File) is a document detailing the whole manufacturing process of BRN 0122410 active pharmaceutical ingredient (API) in detail. Different forms of BRN 0122410 DMFs exist exist since differing nations have different regulations, such as BRN 0122410 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A BRN 0122410 DMF submitted to regulatory agencies in the US is known as a USDMF. BRN 0122410 USDMF includes data on BRN 0122410's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The BRN 0122410 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of BRN 0122410 suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The BRN 0122410 Drug Master File in Japan (BRN 0122410 JDMF) empowers BRN 0122410 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the BRN 0122410 JDMF during the approval evaluation for pharmaceutical products. At the time of BRN 0122410 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of BRN 0122410 suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a BRN 0122410 Drug Master File in Korea (BRN 0122410 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of BRN 0122410. The MFDS reviews the BRN 0122410 KDMF as part of the drug registration process and uses the information provided in the BRN 0122410 KDMF to evaluate the safety and efficacy of the drug.
After submitting a BRN 0122410 KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their BRN 0122410 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of BRN 0122410 suppliers with KDMF on PharmaCompass.
A BRN 0122410 CEP of the European Pharmacopoeia monograph is often referred to as a BRN 0122410 Certificate of Suitability (COS). The purpose of a BRN 0122410 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of BRN 0122410 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of BRN 0122410 to their clients by showing that a BRN 0122410 CEP has been issued for it. The manufacturer submits a BRN 0122410 CEP (COS) as part of the market authorization procedure, and it takes on the role of a BRN 0122410 CEP holder for the record. Additionally, the data presented in the BRN 0122410 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the BRN 0122410 DMF.
A BRN 0122410 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. BRN 0122410 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of BRN 0122410 suppliers with CEP (COS) on PharmaCompass.
A BRN 0122410 written confirmation (BRN 0122410 WC) is an official document issued by a regulatory agency to a BRN 0122410 manufacturer, verifying that the manufacturing facility of a BRN 0122410 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting BRN 0122410 APIs or BRN 0122410 finished pharmaceutical products to another nation, regulatory agencies frequently require a BRN 0122410 WC (written confirmation) as part of the regulatory process.
click here to find a list of BRN 0122410 suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing BRN 0122410 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for BRN 0122410 API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture BRN 0122410 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain BRN 0122410 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a BRN 0122410 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of BRN 0122410 suppliers with NDC on PharmaCompass.
BRN 0122410 Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of BRN 0122410 GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right BRN 0122410 GMP manufacturer or BRN 0122410 GMP API supplier for your needs.
A BRN 0122410 CoA (Certificate of Analysis) is a formal document that attests to BRN 0122410's compliance with BRN 0122410 specifications and serves as a tool for batch-level quality control.
BRN 0122410 CoA mostly includes findings from lab analyses of a specific batch. For each BRN 0122410 CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
BRN 0122410 may be tested according to a variety of international standards, such as European Pharmacopoeia (BRN 0122410 EP), BRN 0122410 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (BRN 0122410 USP).
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