01 1M/s Mylan Laboratories Limited
01 1Pretomanid IH
01 1WC-0016n
01 1India
Date of Issue : 2022-06-15
Valid Till : 2025-06-26
Written Confirmation Number : WC-0016n
Address of the Firm : (Unit IX), Plot No. 5, Road No. 12, Jawahar Nehru Pharma City, Tadi (V), Parawad...
A Pretomanid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pretomanid, including repackagers and relabelers. The FDA regulates Pretomanid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pretomanid API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Pretomanid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pretomanid supplier is an individual or a company that provides Pretomanid active pharmaceutical ingredient (API) or Pretomanid finished formulations upon request. The Pretomanid suppliers may include Pretomanid API manufacturers, exporters, distributors and traders.
click here to find a list of Pretomanid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pretomanid written confirmation (Pretomanid WC) is an official document issued by a regulatory agency to a Pretomanid manufacturer, verifying that the manufacturing facility of a Pretomanid active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Pretomanid APIs or Pretomanid finished pharmaceutical products to another nation, regulatory agencies frequently require a Pretomanid WC (written confirmation) as part of the regulatory process.
click here to find a list of Pretomanid suppliers with Written Confirmation (WC) on PharmaCompass.
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