01 1Divi’s Laboratories
01 1Iopamidol (USP/Ph.Eur/BP)
01 1WC-0031
01 1India
Date of Issue : 2022-06-16
Valid Till : 2025-06-16
Written Confirmation Number : WC-0031
Address of the Firm : Unit-Lingojigudem (V) Choutuppal (M) Nalgonda District Talangana State India
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PharmaCompass offers a list of Iopamidol 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 Iopamidol manufacturer or Iopamidol supplier for your needs.
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A Iopamiron 370 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iopamiron 370, including repackagers and relabelers. The FDA regulates Iopamiron 370 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iopamiron 370 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 Iopamiron 370 supplier is an individual or a company that provides Iopamiron 370 active pharmaceutical ingredient (API) or Iopamiron 370 finished formulations upon request. The Iopamiron 370 suppliers may include Iopamiron 370 API manufacturers, exporters, distributors and traders.
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A Iopamiron 370 written confirmation (Iopamiron 370 WC) is an official document issued by a regulatory agency to a Iopamiron 370 manufacturer, verifying that the manufacturing facility of a Iopamiron 370 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Iopamiron 370 APIs or Iopamiron 370 finished pharmaceutical products to another nation, regulatory agencies frequently require a Iopamiron 370 WC (written confirmation) as part of the regulatory process.
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