01 1M/s. Hetro Labs Limited
01 1Saquinavir Mesylate (Ph. Eur)
01 1WC-0041
01 1India
Date of Issue : 2022-09-16
Valid Till : 2025-08-08
Written Confirmation Number : WC-0041
Address of the Firm : Unit-I, Survey No.10, I.D.A, Gaddapotharam Village, Jinnaram Mandal,Medak Dist, ...
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A Invirase (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Invirase (TN), including repackagers and relabelers. The FDA regulates Invirase (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Invirase (TN) 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 Invirase (TN) supplier is an individual or a company that provides Invirase (TN) active pharmaceutical ingredient (API) or Invirase (TN) finished formulations upon request. The Invirase (TN) suppliers may include Invirase (TN) API manufacturers, exporters, distributors and traders.
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A Invirase (TN) written confirmation (Invirase (TN) WC) is an official document issued by a regulatory agency to a Invirase (TN) manufacturer, verifying that the manufacturing facility of a Invirase (TN) active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Invirase (TN) APIs or Invirase (TN) finished pharmaceutical products to another nation, regulatory agencies frequently require a Invirase (TN) WC (written confirmation) as part of the regulatory process.
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