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