EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1SANOFI WINTHROP INDUSTRIE
01 1Hydroxocobalamin
01 1France
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 226MF10198
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2014-10-27
Latest Date of Registration : 2016-01-08
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PharmaCompass offers a list of Hydroxocobalamin 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 Hydroxocobalamin manufacturer or Hydroxocobalamin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydroxocobalamin manufacturer or Hydroxocobalamin supplier.
A Duradoce manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duradoce, including repackagers and relabelers. The FDA regulates Duradoce manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duradoce 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 Duradoce manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Duradoce supplier is an individual or a company that provides Duradoce active pharmaceutical ingredient (API) or Duradoce finished formulations upon request. The Duradoce suppliers may include Duradoce API manufacturers, exporters, distributors and traders.
click here to find a list of Duradoce 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 Duradoce Drug Master File in Japan (Duradoce JDMF) empowers Duradoce 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 Duradoce JDMF during the approval evaluation for pharmaceutical products. At the time of Duradoce 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 Duradoce suppliers with JDMF on PharmaCompass.
