Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
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01 1Zhejiang Hengkang Pharmaceutical
02 1M/s. Cohance Lifesciences Limited
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01 1Benserazide Hydrochloride
02 1Benserazide Hydrochloride Ph. Eur.
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01 1WC-0150
02 1ZJ230055
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01 1China
02 1India
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Date of Issue : 2023-04-11
Valid Till : 2026-01-26
Written Confirmation Number : ZJ230055
Address of the Firm : No.11 Chengen Road, Pubagang Town, Sanmen, Zhejiang, China 317100
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Benserazide Hydrochloride Ph. Eur.
Date of Issue : 2025-07-24
Valid Till : 2028-07-21
Written Confirmation Number : WC-0150
Address of the Firm : API Unit-l, R.S. No. 50/1, Mukteswarapuram Village, Jaggaiahpet Mandal, NTR Dist...
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A Levodopa and Benserazide-2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levodopa and Benserazide-2, including repackagers and relabelers. The FDA regulates Levodopa and Benserazide-2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levodopa and Benserazide-2 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 Levodopa and Benserazide-2 supplier is an individual or a company that provides Levodopa and Benserazide-2 active pharmaceutical ingredient (API) or Levodopa and Benserazide-2 finished formulations upon request. The Levodopa and Benserazide-2 suppliers may include Levodopa and Benserazide-2 API manufacturers, exporters, distributors and traders.
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A Levodopa and Benserazide-2 written confirmation (Levodopa and Benserazide-2 WC) is an official document issued by a regulatory agency to a Levodopa and Benserazide-2 manufacturer, verifying that the manufacturing facility of a Levodopa and Benserazide-2 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Levodopa and Benserazide-2 APIs or Levodopa and Benserazide-2 finished pharmaceutical products to another nation, regulatory agencies frequently require a Levodopa and Benserazide-2 WC (written confirmation) as part of the regulatory process.
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