01 1M/s. Souvin Pharmaceuticals(l) Pvt. Ltd
01 1Coumarin (GP)
01 1WC-270
01 1India
Date of Issue : 2023-08-14
Valid Till : 2026-08-14
Written Confirmation Number : WC-270
Address of the Firm : Gat No.1170, Ghotawade, Tal-Mulshi, Dist. Pune-411042, Maharashtra
91
PharmaCompass offers a list of Coumarin 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 Coumarin manufacturer or Coumarin supplier for your needs.
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A CUMARINA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CUMARINA, including repackagers and relabelers. The FDA regulates CUMARINA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CUMARINA 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 CUMARINA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CUMARINA supplier is an individual or a company that provides CUMARINA active pharmaceutical ingredient (API) or CUMARINA finished formulations upon request. The CUMARINA suppliers may include CUMARINA API manufacturers, exporters, distributors and traders.
click here to find a list of CUMARINA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CUMARINA written confirmation (CUMARINA WC) is an official document issued by a regulatory agency to a CUMARINA manufacturer, verifying that the manufacturing facility of a CUMARINA active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting CUMARINA APIs or CUMARINA finished pharmaceutical products to another nation, regulatory agencies frequently require a CUMARINA WC (written confirmation) as part of the regulatory process.
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