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