Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
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Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Date of Issue : 2022-04-28
Valid Till : 2024-12-15
Written Confirmation Number : ZJ220039
Address of the Firm : No.11 Chengen Road, Pubagang Town, Sanmen, Zhejiang, China 317108
Date of Issue : 2022-05-18
Valid Till : 2025-05-28
Written Confirmation Number : WC-0019
Address of the Firm : Plot No: 115, Ramky Pharma City (India) Ltd. SEZ, Parawada Mandal, Visakhapatnam...
Date of Issue : 2022-05-18
Valid Till : 2025-05-28
Written Confirmation Number : WC-0019
Address of the Firm : Plot No: 115, Ramky Pharma City (India) Ltd. SEZ, Parawada Mandal, Visakhapatnam...
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PharmaCompass offers a list of Mesalazine 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 Mesalazine manufacturer or Mesalazine supplier for your needs.
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A Mesalazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mesalazine, including repackagers and relabelers. The FDA regulates Mesalazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mesalazine 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 Mesalazine supplier is an individual or a company that provides Mesalazine active pharmaceutical ingredient (API) or Mesalazine finished formulations upon request. The Mesalazine suppliers may include Mesalazine API manufacturers, exporters, distributors and traders.
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A Mesalazine written confirmation (Mesalazine WC) is an official document issued by a regulatory agency to a Mesalazine manufacturer, verifying that the manufacturing facility of a Mesalazine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Mesalazine APIs or Mesalazine finished pharmaceutical products to another nation, regulatory agencies frequently require a Mesalazine WC (written confirmation) as part of the regulatory process.
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