01 1M/s. Cipla Ltd.
01 1Cyproterone Acetate (BP/EP)
01 1WC-0140
01 1India
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
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A Cyprostat® manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyprostat®, including repackagers and relabelers. The FDA regulates Cyprostat® manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyprostat® 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 Cyprostat® supplier is an individual or a company that provides Cyprostat® active pharmaceutical ingredient (API) or Cyprostat® finished formulations upon request. The Cyprostat® suppliers may include Cyprostat® API manufacturers, exporters, distributors and traders.
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A Cyprostat® written confirmation (Cyprostat® WC) is an official document issued by a regulatory agency to a Cyprostat® manufacturer, verifying that the manufacturing facility of a Cyprostat® active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Cyprostat® APIs or Cyprostat® finished pharmaceutical products to another nation, regulatory agencies frequently require a Cyprostat® WC (written confirmation) as part of the regulatory process.
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