EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1SANOFI WINTHROP INDUSTRIE
01 1Birds Mi plug Min maleate
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 Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trimipramine Maleate, including repackagers and relabelers. The FDA regulates Trimipramine Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trimipramine Maleate 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 Maleate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trimipramine Maleate supplier is an individual or a company that provides Trimipramine Maleate active pharmaceutical ingredient (API) or Trimipramine Maleate finished formulations upon request. The Trimipramine Maleate suppliers may include Trimipramine Maleate API manufacturers, exporters, distributors and traders.
click here to find a list of Trimipramine Maleate 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 Maleate Drug Master File in Japan (Trimipramine Maleate JDMF) empowers Trimipramine Maleate 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 Maleate JDMF during the approval evaluation for pharmaceutical products. At the time of Trimipramine Maleate 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 Maleate suppliers with JDMF on PharmaCompass.
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