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
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PharmaCompass offers a list of Clobazam API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Clobazam manufacturer or Clobazam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clobazam manufacturer or Clobazam supplier.
PharmaCompass also assists you with knowing the Clobazam API Price utilized in the formulation of products. Clobazam API Price is not always fixed or binding as the Clobazam Price is obtained through a variety of data sources. The Clobazam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Noiafren manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Noiafren, including repackagers and relabelers. The FDA regulates Noiafren manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Noiafren 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 Noiafren manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Noiafren supplier is an individual or a company that provides Noiafren active pharmaceutical ingredient (API) or Noiafren finished formulations upon request. The Noiafren suppliers may include Noiafren API manufacturers, exporters, distributors and traders.
click here to find a list of Noiafren 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 Noiafren Drug Master File in Japan (Noiafren JDMF) empowers Noiafren 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 Noiafren JDMF during the approval evaluation for pharmaceutical products. At the time of Noiafren 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 Noiafren suppliers with JDMF on PharmaCompass.
