01 1M/s. Hetro Labs Limited
01 1Crizotinib IH
01 1WC-0041
01 1India
Date of Issue : 2022-09-16
Valid Till : 2025-08-08
Written Confirmation Number : WC-0041
Address of the Firm : Unit-I, Survey No.10, I.D.A, Gaddapotharam Village, Jinnaram Mandal,Medak Dist, ...
A Crizotinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Crizotinib, including repackagers and relabelers. The FDA regulates Crizotinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Crizotinib 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 Crizotinib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Crizotinib supplier is an individual or a company that provides Crizotinib active pharmaceutical ingredient (API) or Crizotinib finished formulations upon request. The Crizotinib suppliers may include Crizotinib API manufacturers, exporters, distributors and traders.
click here to find a list of Crizotinib suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Crizotinib written confirmation (Crizotinib WC) is an official document issued by a regulatory agency to a Crizotinib manufacturer, verifying that the manufacturing facility of a Crizotinib active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Crizotinib APIs or Crizotinib finished pharmaceutical products to another nation, regulatory agencies frequently require a Crizotinib WC (written confirmation) as part of the regulatory process.
click here to find a list of Crizotinib suppliers with Written Confirmation (WC) on PharmaCompass.
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