Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
01 1Syn-Tech Chem & Pharm Co., Ltd.
02 2M/s Alembic Pharmaceuticals limited
03 1M/s Glenmark Life Sciences Limited
04 1M/s Natco Pharma Limited
05 1M/s SMS Pharmaceuticals Limited
06 1M/s Sun Pharmaceuticals Industries ltd
07 1M/s Unichem Laboratories Limited
08 1M/s. Apitoria Pharma Private Limited
09 1M/s. Jubilant Biosys Limited
10 1M/s. Nosch Labs Pvt. Ltd.
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Date of Issue : 2022-02-22
Valid Till : 2025-07-15
Written Confirmation Number : TFDA-0002291
Address of the Firm : No. 168, Kai Yuan Rd, Hsin-Ying, Tainan City 73055, Taiwan
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PharmaCompass offers a list of Zolmitriptan API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Zolmitriptan manufacturer or Zolmitriptan supplier for your needs.
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A Zomitan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zomitan, including repackagers and relabelers. The FDA regulates Zomitan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zomitan API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Zomitan supplier is an individual or a company that provides Zomitan active pharmaceutical ingredient (API) or Zomitan finished formulations upon request. The Zomitan suppliers may include Zomitan API manufacturers, exporters, distributors and traders.
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A Zomitan written confirmation (Zomitan WC) is an official document issued by a regulatory agency to a Zomitan manufacturer, verifying that the manufacturing facility of a Zomitan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Zomitan APIs or Zomitan finished pharmaceutical products to another nation, regulatory agencies frequently require a Zomitan WC (written confirmation) as part of the regulatory process.
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