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 Isovue 370 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Isovue 370, including repackagers and relabelers. The FDA regulates Isovue 370 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Isovue 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 Isovue 370 supplier is an individual or a company that provides Isovue 370 active pharmaceutical ingredient (API) or Isovue 370 finished formulations upon request. The Isovue 370 suppliers may include Isovue 370 API manufacturers, exporters, distributors and traders.
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A Isovue 370 written confirmation (Isovue 370 WC) is an official document issued by a regulatory agency to a Isovue 370 manufacturer, verifying that the manufacturing facility of a Isovue 370 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Isovue 370 APIs or Isovue 370 finished pharmaceutical products to another nation, regulatory agencies frequently require a Isovue 370 WC (written confirmation) as part of the regulatory process.
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