EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI Germany GmbH
01 1Clobazam
01 1France
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 218MF10337
Registrant's Address : Brueningstrasse 50, 65926 Frankfurt am Main, Germany
Initial Date of Registration : 2006-03-09
Latest Date of Registration : 2010-01-07
A Clobazam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clobazam, including repackagers and relabelers. The FDA regulates Clobazam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clobazam 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 Clobazam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clobazam supplier is an individual or a company that provides Clobazam active pharmaceutical ingredient (API) or Clobazam finished formulations upon request. The Clobazam suppliers may include Clobazam API manufacturers, exporters, distributors and traders.
click here to find a list of Clobazam 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 Clobazam Drug Master File in Japan (Clobazam JDMF) empowers Clobazam 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 Clobazam JDMF during the approval evaluation for pharmaceutical products. At the time of Clobazam 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 Clobazam suppliers with JDMF on PharmaCompass.
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