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
PharmaCompass offers a list of Acemetacin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Acemetacin manufacturer or Acemetacin supplier for your needs.
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PharmaCompass also assists you with knowing the Acemetacin API Price utilized in the formulation of products. Acemetacin API Price is not always fixed or binding as the Acemetacin Price is obtained through a variety of data sources. The Acemetacin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Acemetacin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acemetacin, including repackagers and relabelers. The FDA regulates Acemetacin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acemetacin 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 supplier is an individual or a company that provides Acemetacin active pharmaceutical ingredient (API) or Acemetacin finished formulations upon request. The Acemetacin suppliers may include Acemetacin API manufacturers, exporters, distributors and traders.
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A Acemetacin written confirmation (Acemetacin WC) is an official document issued by a regulatory agency to a Acemetacin manufacturer, verifying that the manufacturing facility of a Acemetacin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Acemetacin APIs or Acemetacin finished pharmaceutical products to another nation, regulatory agencies frequently require a Acemetacin WC (written confirmation) as part of the regulatory process.
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