EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1SANOFI WINTHROP INDUSTRIE
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01 1France
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 220MF10195
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2008-08-28
Latest Date of Registration : 2012-04-25
A Trimipramine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trimipramine, including repackagers and relabelers. The FDA regulates Trimipramine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trimipramine 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 Trimipramine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trimipramine supplier is an individual or a company that provides Trimipramine active pharmaceutical ingredient (API) or Trimipramine finished formulations upon request. The Trimipramine suppliers may include Trimipramine API manufacturers, exporters, distributors and traders.
click here to find a list of Trimipramine 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 Trimipramine Drug Master File in Japan (Trimipramine JDMF) empowers Trimipramine 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 Trimipramine JDMF during the approval evaluation for pharmaceutical products. At the time of Trimipramine 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 Trimipramine suppliers with JDMF on PharmaCompass.
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