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
Maithri Drugs: Delivering Trusted, High-Quality APIs to 35+ Countries with Innovation, Compliance, and Excellence.
Date of Issue : 2024-02-12
Valid Till : 2027-02-11
Written Confirmation Number : WC-0407
Address of the Firm : Sy. No. 205, 222 to 226, IDA Bonthapally, Bonthapally (Village), Gummadidala (Ma...
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A Apriso manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Apriso, including repackagers and relabelers. The FDA regulates Apriso manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Apriso 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 Apriso supplier is an individual or a company that provides Apriso active pharmaceutical ingredient (API) or Apriso finished formulations upon request. The Apriso suppliers may include Apriso API manufacturers, exporters, distributors and traders.
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A Apriso written confirmation (Apriso WC) is an official document issued by a regulatory agency to a Apriso manufacturer, verifying that the manufacturing facility of a Apriso active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Apriso APIs or Apriso finished pharmaceutical products to another nation, regulatory agencies frequently require a Apriso WC (written confirmation) as part of the regulatory process.
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