01 1MSN Laboratories Pvt. Ltd.
01 1Dacomitinib Monohydrate IH
01 1WC-0349
01 1India
Date of Issue : 2022-09-02
Valid Till : 2025-05-05
Written Confirmation Number : WC-0349
Address of the Firm : MIs. MSN Laboratories Private Limited, Unit-II, sv. No, 50, Kardanur (Village), ...
A Dacomitinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dacomitinib, including repackagers and relabelers. The FDA regulates Dacomitinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dacomitinib 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 Dacomitinib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dacomitinib supplier is an individual or a company that provides Dacomitinib active pharmaceutical ingredient (API) or Dacomitinib finished formulations upon request. The Dacomitinib suppliers may include Dacomitinib API manufacturers, exporters, distributors and traders.
click here to find a list of Dacomitinib suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dacomitinib written confirmation (Dacomitinib WC) is an official document issued by a regulatory agency to a Dacomitinib manufacturer, verifying that the manufacturing facility of a Dacomitinib active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dacomitinib APIs or Dacomitinib finished pharmaceutical products to another nation, regulatory agencies frequently require a Dacomitinib WC (written confirmation) as part of the regulatory process.
click here to find a list of Dacomitinib suppliers with Written Confirmation (WC) on PharmaCompass.
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