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...
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PharmaCompass offers a list of Etofenamate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Etofenamate manufacturer or Etofenamate supplier for your needs.
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PharmaCompass also assists you with knowing the Etofenamate API Price utilized in the formulation of products. Etofenamate API Price is not always fixed or binding as the Etofenamate Price is obtained through a variety of data sources. The Etofenamate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bayro manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bayro, including repackagers and relabelers. The FDA regulates Bayro manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bayro API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Bayro written confirmation (Bayro WC) is an official document issued by a regulatory agency to a Bayro manufacturer, verifying that the manufacturing facility of a Bayro active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Bayro APIs or Bayro finished pharmaceutical products to another nation, regulatory agencies frequently require a Bayro WC (written confirmation) as part of the regulatory process.
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