EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 222MF10114
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2010-03-25
Latest Date of Registration : 2010-03-25
A Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Succinate, including repackagers and relabelers. The FDA regulates Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Succinate 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 Succinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Succinate supplier is an individual or a company that provides Succinate active pharmaceutical ingredient (API) or Succinate finished formulations upon request. The Succinate suppliers may include Succinate API manufacturers, exporters, distributors and traders.
click here to find a list of Succinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Succinate Drug Master File in Japan (Succinate JDMF) empowers Succinate 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 Succinate JDMF during the approval evaluation for pharmaceutical products. At the time of Succinate 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 Succinate suppliers with JDMF on PharmaCompass.
LOOKING FOR A SUPPLIER?
