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
85
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A Azeat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azeat, including repackagers and relabelers. The FDA regulates Azeat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azeat 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 Azeat supplier is an individual or a company that provides Azeat active pharmaceutical ingredient (API) or Azeat finished formulations upon request. The Azeat suppliers may include Azeat API manufacturers, exporters, distributors and traders.
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A Azeat written confirmation (Azeat WC) is an official document issued by a regulatory agency to a Azeat manufacturer, verifying that the manufacturing facility of a Azeat active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Azeat APIs or Azeat finished pharmaceutical products to another nation, regulatory agencies frequently require a Azeat WC (written confirmation) as part of the regulatory process.
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