01 1M/s. Mylan Lab Ltd.
01 1Erlotinib HCL (INH)
01 1WC-0157
01 1India
Date of Issue : 2019-10-11
Valid Till : 2022-07-02
Written Confirmation Number : WC-0157
Address of the Firm : Plot No. 1A/2, MIDC, Taloja, Panvel, Dist. Raigad, Maharashtra State
A Erlotinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Erlotinib, including repackagers and relabelers. The FDA regulates Erlotinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Erlotinib 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 Erlotinib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Erlotinib supplier is an individual or a company that provides Erlotinib active pharmaceutical ingredient (API) or Erlotinib finished formulations upon request. The Erlotinib suppliers may include Erlotinib API manufacturers, exporters, distributors and traders.
click here to find a list of Erlotinib suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Erlotinib written confirmation (Erlotinib WC) is an official document issued by a regulatory agency to a Erlotinib manufacturer, verifying that the manufacturing facility of a Erlotinib active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Erlotinib APIs or Erlotinib finished pharmaceutical products to another nation, regulatory agencies frequently require a Erlotinib WC (written confirmation) as part of the regulatory process.
click here to find a list of Erlotinib suppliers with Written Confirmation (WC) on PharmaCompass.
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