01 1M/s. Sterling Biotech Limited
01 1Daunorubicine Hydrochloride (Ph.Eur)
01 1WC-0292
01 1India
Daunorubicine Hydrochloride (Ph.Eur)
Date of Issue : 2020-12-18
Valid Till : 2023-12-17
Written Confirmation Number : WC-0292
Address of the Firm : Jambusar State Highway, Village-Masar-391421, Tal- Padra, Dist. Vadodara
A Daunorubicin HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Daunorubicin HCl, including repackagers and relabelers. The FDA regulates Daunorubicin HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Daunorubicin HCl 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 Daunorubicin HCl supplier is an individual or a company that provides Daunorubicin HCl active pharmaceutical ingredient (API) or Daunorubicin HCl finished formulations upon request. The Daunorubicin HCl suppliers may include Daunorubicin HCl API manufacturers, exporters, distributors and traders.
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A Daunorubicin HCl written confirmation (Daunorubicin HCl WC) is an official document issued by a regulatory agency to a Daunorubicin HCl manufacturer, verifying that the manufacturing facility of a Daunorubicin HCl active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Daunorubicin HCl APIs or Daunorubicin HCl finished pharmaceutical products to another nation, regulatory agencies frequently require a Daunorubicin HCl WC (written confirmation) as part of the regulatory process.
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