01 1Henan Quanyu Pharmaceutical Co. , Ltd.
01 1Tiopronin
01 1China
Registration Number : 303MF10092
Registrant's Address : Industrial Park, Neixiang County, Nanyang City, Henan, China
Initial Date of Registration : 2021-06-09
Latest Date of Registration : 2021-06-09
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PharmaCompass offers a list of Tiopronin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Tiopronin manufacturer or Tiopronin supplier for your needs.
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A Vincol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vincol, including repackagers and relabelers. The FDA regulates Vincol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vincol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Vincol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Vincol supplier is an individual or a company that provides Vincol active pharmaceutical ingredient (API) or Vincol finished formulations upon request. The Vincol suppliers may include Vincol API manufacturers, exporters, distributors and traders.
click here to find a list of Vincol suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Vincol Drug Master File in Japan (Vincol JDMF) empowers Vincol API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Vincol JDMF during the approval evaluation for pharmaceutical products. At the time of Vincol JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Vincol suppliers with JDMF on PharmaCompass.
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