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