Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
01 1Zhejiang Hengkang Pharmaceutical
01 1Acemetacin
01 1ZJ230010
01 1China
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Date of Issue : 2023-01-18
Valid Till : 2026-01-17
Written Confirmation Number : ZJ230010
Address of the Firm : No.11 Chengen Road, Pubagang Town, Sanmen, Zhejiang, China 317100
69
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A Acemetacin intermuti manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acemetacin intermuti, including repackagers and relabelers. The FDA regulates Acemetacin intermuti manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acemetacin intermuti 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 Acemetacin intermuti supplier is an individual or a company that provides Acemetacin intermuti active pharmaceutical ingredient (API) or Acemetacin intermuti finished formulations upon request. The Acemetacin intermuti suppliers may include Acemetacin intermuti API manufacturers, exporters, distributors and traders.
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A Acemetacin intermuti written confirmation (Acemetacin intermuti WC) is an official document issued by a regulatory agency to a Acemetacin intermuti manufacturer, verifying that the manufacturing facility of a Acemetacin intermuti active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Acemetacin intermuti APIs or Acemetacin intermuti finished pharmaceutical products to another nation, regulatory agencies frequently require a Acemetacin intermuti WC (written confirmation) as part of the regulatory process.
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