01 1M/s. Biocon Limited
02 1M/s. Concord Biotech Ltd.,
01 2Temsirolimus IH
01 1WC-0100N1
02 1WC-0111
01 2India
Date of Issue : 2022-05-06
Valid Till : 2025-07-02
Written Confirmation Number : WC-0100N1
Address of the Firm : Plot Number 2,3,4 & 5, Phase-IV, Bommasandra-Jigani Link Road, Bommasandra Post,...
Date of Issue : 2022-12-16
Valid Till : 2025-07-02
Written Confirmation Number : WC-0111
Address of the Firm : Survay No. 1482-1486,Trasad Road, Dholka, Dist:- Ahmedabad-382225, Gujarat
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A Temsirolimus - Torisel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Temsirolimus - Torisel, including repackagers and relabelers. The FDA regulates Temsirolimus - Torisel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Temsirolimus - Torisel 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 Temsirolimus - Torisel supplier is an individual or a company that provides Temsirolimus - Torisel active pharmaceutical ingredient (API) or Temsirolimus - Torisel finished formulations upon request. The Temsirolimus - Torisel suppliers may include Temsirolimus - Torisel API manufacturers, exporters, distributors and traders.
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A Temsirolimus - Torisel written confirmation (Temsirolimus - Torisel WC) is an official document issued by a regulatory agency to a Temsirolimus - Torisel manufacturer, verifying that the manufacturing facility of a Temsirolimus - Torisel active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Temsirolimus - Torisel APIs or Temsirolimus - Torisel finished pharmaceutical products to another nation, regulatory agencies frequently require a Temsirolimus - Torisel WC (written confirmation) as part of the regulatory process.
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