EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI FRANCE
01 1Methyl succinate
01 1France
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 220MF10128
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2008-05-15
Latest Date of Registration : 2019-03-05
A Methylprednisolone Hemisuccinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methylprednisolone Hemisuccinate, including repackagers and relabelers. The FDA regulates Methylprednisolone Hemisuccinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methylprednisolone Hemisuccinate 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 Methylprednisolone Hemisuccinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methylprednisolone Hemisuccinate supplier is an individual or a company that provides Methylprednisolone Hemisuccinate active pharmaceutical ingredient (API) or Methylprednisolone Hemisuccinate finished formulations upon request. The Methylprednisolone Hemisuccinate suppliers may include Methylprednisolone Hemisuccinate API manufacturers, exporters, distributors and traders.
click here to find a list of Methylprednisolone Hemisuccinate 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 Methylprednisolone Hemisuccinate Drug Master File in Japan (Methylprednisolone Hemisuccinate JDMF) empowers Methylprednisolone Hemisuccinate 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 Methylprednisolone Hemisuccinate JDMF during the approval evaluation for pharmaceutical products. At the time of Methylprednisolone Hemisuccinate 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 Methylprednisolone Hemisuccinate suppliers with JDMF on PharmaCompass.
We have 1 companies offering Methylprednisolone Hemisuccinate
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
