01 1M/s. Cipla Ltd.
01 1Tenofovir Hydrochloride (BP/Ph. Eur.)
01 1WC-0140
01 1India
Tenofovir Hydrochloride (BP/Ph. Eur.)
Date of Issue : 2022-06-03
Valid Till : 2025-07-02
Written Confirmation Number : WC-0140
Address of the Firm : D-22, MIDC, Kurkumbh, Dist. Pune-413 802
53
PharmaCompass offers a list of Tenofovir 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 Tenofovir manufacturer or Tenofovir supplier for your needs.
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A CS-1609 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CS-1609, including repackagers and relabelers. The FDA regulates CS-1609 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CS-1609 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 CS-1609 supplier is an individual or a company that provides CS-1609 active pharmaceutical ingredient (API) or CS-1609 finished formulations upon request. The CS-1609 suppliers may include CS-1609 API manufacturers, exporters, distributors and traders.
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A CS-1609 written confirmation (CS-1609 WC) is an official document issued by a regulatory agency to a CS-1609 manufacturer, verifying that the manufacturing facility of a CS-1609 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting CS-1609 APIs or CS-1609 finished pharmaceutical products to another nation, regulatory agencies frequently require a CS-1609 WC (written confirmation) as part of the regulatory process.
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