01 1M/s Polypeptide laboratories Pvt ltd
01 1Triptorelin IH
01 1WC-0047a3
01 1India
Date of Issue : 2020-01-28
Valid Till : 2022-06-27
Written Confirmation Number : WC-0047a3
Address of the Firm : K-28, MIDC, Anandnagar, Ambernath (E), Thane-421 506
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PharmaCompass offers a list of Triptorelin 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 Triptorelin manufacturer or Triptorelin supplier for your needs.
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A Pamorelin LA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pamorelin LA, including repackagers and relabelers. The FDA regulates Pamorelin LA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pamorelin LA 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 Pamorelin LA supplier is an individual or a company that provides Pamorelin LA active pharmaceutical ingredient (API) or Pamorelin LA finished formulations upon request. The Pamorelin LA suppliers may include Pamorelin LA API manufacturers, exporters, distributors and traders.
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A Pamorelin LA written confirmation (Pamorelin LA WC) is an official document issued by a regulatory agency to a Pamorelin LA manufacturer, verifying that the manufacturing facility of a Pamorelin LA active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Pamorelin LA APIs or Pamorelin LA finished pharmaceutical products to another nation, regulatory agencies frequently require a Pamorelin LA WC (written confirmation) as part of the regulatory process.
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