01 1M/s Aurore Pharmaceuticals Private Limited
01 1Camostat Mesilate JP
01 1WC-0119
01 1India
Date of Issue : 2022-09-19
Valid Till : 2025-07-02
Written Confirmation Number : WC-0119
Address of the Firm : Plot No. 35, 36, 38, 39,40,49, 50 & 51, Phase-IV, IDA, Jeedimetla, Medchal- Malk...
A Camostat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Camostat, including repackagers and relabelers. The FDA regulates Camostat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Camostat 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 Camostat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Camostat supplier is an individual or a company that provides Camostat active pharmaceutical ingredient (API) or Camostat finished formulations upon request. The Camostat suppliers may include Camostat API manufacturers, exporters, distributors and traders.
click here to find a list of Camostat suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Camostat written confirmation (Camostat WC) is an official document issued by a regulatory agency to a Camostat manufacturer, verifying that the manufacturing facility of a Camostat active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Camostat APIs or Camostat finished pharmaceutical products to another nation, regulatory agencies frequently require a Camostat WC (written confirmation) as part of the regulatory process.
click here to find a list of Camostat suppliers with Written Confirmation (WC) on PharmaCompass.
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