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 1M/s Glenmark Life Sciences Limited
03 1M/s Jubilant Pharmova Limited
04 2M/s Natco Pharma Limited
05 1M/s SMS Pharmaceuticals Limited
06 1M/s Sun Pharmaceuticals Industries ltd
07 1M/s Tianish Laboratories Privte Lmited
08 1M/s Unichem Laboratories Limited
09 1M/s. Apitoria Pharma Private Limited
10 2M/sAlembic Pharmaceuticals limited
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 Zolmiles manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zolmiles, including repackagers and relabelers. The FDA regulates Zolmiles manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zolmiles 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 Zolmiles supplier is an individual or a company that provides Zolmiles active pharmaceutical ingredient (API) or Zolmiles finished formulations upon request. The Zolmiles suppliers may include Zolmiles API manufacturers, exporters, distributors and traders.
click here to find a list of Zolmiles suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zolmiles written confirmation (Zolmiles WC) is an official document issued by a regulatory agency to a Zolmiles manufacturer, verifying that the manufacturing facility of a Zolmiles active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Zolmiles APIs or Zolmiles finished pharmaceutical products to another nation, regulatory agencies frequently require a Zolmiles WC (written confirmation) as part of the regulatory process.
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