01 1M/s Alivus Life Sciences Limited
01 1Sertaconazole Nitrate BP/Ph.Eur
01 1WC-0310
01 1India
Sertaconazole Nitrate BP/Ph.Eur
Date of Issue : 2023-11-28
Valid Till : 2026-11-28
Written Confirmation Number : WC-0310
Address of the Firm : Plot No. Z-103/l, Dahej SEZ, Phase II, Dahej, Dist-Bharuch, Gujarat, India
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A Dermoseptic manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dermoseptic, including repackagers and relabelers. The FDA regulates Dermoseptic manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dermoseptic 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 Dermoseptic supplier is an individual or a company that provides Dermoseptic active pharmaceutical ingredient (API) or Dermoseptic finished formulations upon request. The Dermoseptic suppliers may include Dermoseptic API manufacturers, exporters, distributors and traders.
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A Dermoseptic written confirmation (Dermoseptic WC) is an official document issued by a regulatory agency to a Dermoseptic manufacturer, verifying that the manufacturing facility of a Dermoseptic active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dermoseptic APIs or Dermoseptic finished pharmaceutical products to another nation, regulatory agencies frequently require a Dermoseptic WC (written confirmation) as part of the regulatory process.
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