01 1M/s. Dishman Pharmaceuticals and Chemicals Ltd.
01 1Etofenamate Ph.Eur
01 1WC-0135
01 1India
Date of Issue : 2019-07-22
Valid Till : 2022-07-02
Written Confirmation Number : WC-0135
Address of the Firm : Survey No. 47, Paiki Sub Plot No. 1, Village Lodariyal, Taluka Sanand, Dist. Ahm...
A Etofenamate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etofenamate, including repackagers and relabelers. The FDA regulates Etofenamate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etofenamate 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 Etofenamate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etofenamate supplier is an individual or a company that provides Etofenamate active pharmaceutical ingredient (API) or Etofenamate finished formulations upon request. The Etofenamate suppliers may include Etofenamate API manufacturers, exporters, distributors and traders.
click here to find a list of Etofenamate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etofenamate written confirmation (Etofenamate WC) is an official document issued by a regulatory agency to a Etofenamate manufacturer, verifying that the manufacturing facility of a Etofenamate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Etofenamate APIs or Etofenamate finished pharmaceutical products to another nation, regulatory agencies frequently require a Etofenamate WC (written confirmation) as part of the regulatory process.
click here to find a list of Etofenamate suppliers with Written Confirmation (WC) on PharmaCompass.
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