06 May 2022

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Carvedilol Impurity needed in India [ENA13539]
A company based in India that deals in the trading of various pharmaceutical products is looking for suppliers of Carvedilol Impurity for commercial purpose. The suppliers must support this enquiry with CoA.

Comments :

yangxiaoqing2@ncpc.biz

NCPC, one of the largest pharmaceutical enterprise in China can meet your requirements. Please send the detailed inquiry to yangxiaoqing2@ncpc.biz.

11:35,  06 May 2022

yangxiaoqing2@ncpc.biz

NCPC, one of the largest pharmaceutical enterprise in China can meet your requirements. Please send the detailed inquiry to yangxiaoqing2@ncpc.biz.

11:35,  06 May 2022

yangxiaoqing2@ncpc.biz

NCPC, one of the largest pharmaceutical enterprise in China can meet your requirements. Please send the detailed inquiry to yangxiaoqing2@ncpc.biz.

11:35,  06 May 2022

alicechan@huarizy.com

HUNAN HUARI PHARMACEUTICAL CO.,LTD. is the Chinese manufacturer for the following APIs and excipients, please feel free to contact us if you have any requirements.

1) Citric acid Monohydrate GMP
2) Citric acid Anhydrous GMP
3) Sodium citrate GMP
4) Potassium Citrate GMP
5) Sodium benzoate
6) Stearic acid
7) Sodium cyclamate
8) Potassium Sorbate
9) Polysorbate 80

email address: alicechan@huarizy.com
phone number: +86 18820220687

12:00,  06 May 2022

info@indeximinternational.com

INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard, Impurities, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements, silica gel, Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian, Ukraine, Russia, and also a few products to Australia, UK & USA.
We are also contract manufacturer of APIs and attached is the list of products and by cooperation with other manufacturers in India. Also, most of the products are from WHO cGMP, ISO, GMP manufacturers.
sales.indeximinternational@gmail.com
info@indeximinternational.com
www.indexim.in
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVED

13:21,  06 May 2022

info@indeximinternational.com

INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard, Impurities, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements, silica gel, Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian, Ukraine, Russia, and also a few products to Australia, UK & USA.
We are also contract manufacturer of APIs and attached is the list of products and by cooperation with other manufacturers in India. Also, most of the products are from WHO cGMP, ISO, GMP manufacturers.
sales.indeximinternational@gmail.com
info@indeximinternational.com
www.indexim.in
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVED

13:21,  06 May 2022

alicia@aozeal.com

info@indeximinternational.com

INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard, Impurities, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements, silica gel, Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian, Ukraine, Russia, and also a few products to Australia, UK & USA.
We are also contract manufacturer of APIs and attached is the list of products and by cooperation with other manufacturers in India. Also, most of the products are from WHO cGMP, ISO, GMP manufacturers.
sales.indeximinternational@gmail.com
info@indeximinternational.com
www.indexim.in
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVED

10:23, 21 Apr 2022
alicechan@huarizy.com

HUNAN HUARI PHARMACEUTICAL CO.,LTD. is the Chinese manufacturer for the following APIs and excipients, please feel free to contact us if you have any requirements.

1) Citric acid Monohydrate GMP
2) Citric acid Anhydrous GMP
3) Sodium citrate GMP
4) Potassium Citrate GMP
5) Sodium benzoate
6) Stearic acid
7) Sodium cyclamate
8) Potassium Sorbate
9) Polysorbate 80

email address: alicechan@huarizy.com
phone number: +86 18820220687

12:02, 21 Apr 2022
navee@chemyzolab.com

Please contact us for your requirements to navee@chemyzolab.com/naveechemyzola@gmail.com

13:10, 21 Apr 2022
navee@chemyzolab.com

Please contact us for your requirements to navee@chemyzolab.com/naveechemyzola@gmail.com

13:10, 21 Apr 2022
alicia@aozeal.com

Aozeal Certified Standards (AOCS), Inc. is a
high-tech bio-pharmaceutical company
specialized in synthesis and supply of API
impurities and other pharmaceutical
reference standards with customers’ desired
purity, characterization and QTY. We are
engaged in the business of pharmaceutical
reference standards for many years

06:25,  09 May 2022

himali.pawaskar@dksh.com

Hi , please share this lead

11:47,  11 May 2022

hostrinlifesciences@gmail.com

Dear friend,

Greetings from Hostrin Life Sciences!!!

We have been supporting the following services.

1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA. DMF's for API's, Tech transfer support and Registration of Dossiers in MOH /MHRA/EMEA/FDA with 5 modules including BA and BE studies /Clinical studies/trials for finished formulation's in Pharmaceutical, ayurveda, Biotech, Biosimilar, vitamins , Peptides and Transdermal patches too.

2. eCTD publishing with potential software, addressing post submission queries from all regulatory authorities and all type of mock audits like USFDA_21_CFR with GAP filling for USFDA, WHO-GMP, EU-GMP, MHRA, TGA, PMDA and PICS audits as well.

3. Impurity's & Reference standards support for API's

4. Services for IPR & Regulatory compliance

5. Services for QMS & supporting of QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars companies who are willing to enter into the Regulatory market which is mandatory to show for FDA.

6. Custom synthesis and contract manufacturing services

7. Synthetic Resins technologies support.

8. Cleaning validation/ toxicology studies reports (PD values) for commercial manufacturing of APIs and finished formulations.

9. Pharmacovigilance services.

Pls don't hesitate to send your inquiries. For your reference, please go through our website www.hostringlobal.com

Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343

22:48,  11 May 2022

sunil.sykem@protonmail.com

SYKEM Pharma Research and Development we are leading manufacturer of Nitroso amine and API Impurities

Company purely work on organic synthesis as a Custom CRO, Impurity synthesis and Intermediate synthesis .Introducing here Company profile along with commercials for available impurities,

We synthesis API intermediate in KG Scale if you need any intermediate or lab chemical or HPLC, GC, KF, chemicals please contact us we are willing to supply

Also, we have fully developed ADL (Analytical development laboratory), for sample analysis, if you have a sample for analysis please find our sample analysis price list, we are happy to provide you with the best service for sample analysis.
sunil.sykem@protonmail.com
info@sykempharma.com

17:56,  30 Jul 2022
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