EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI ITALY S. r. l.
01 1Rifampicin
01 1France
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 218MF10388
Registrant's Address : Via Angelo Titi, 22/26, Zona ex punto franco, 72100 Brindisi, Italy
Initial Date of Registration : 2006-03-20
Latest Date of Registration : 2025-08-21
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PharmaCompass offers a list of Rifampicin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Rifampicin manufacturer or Rifampicin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rifampicin manufacturer or Rifampicin supplier.
A Rifampicin & EEP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rifampicin & EEP, including repackagers and relabelers. The FDA regulates Rifampicin & EEP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rifampicin & EEP 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 Rifampicin & EEP manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Rifampicin & EEP supplier is an individual or a company that provides Rifampicin & EEP active pharmaceutical ingredient (API) or Rifampicin & EEP finished formulations upon request. The Rifampicin & EEP suppliers may include Rifampicin & EEP API manufacturers, exporters, distributors and traders.
click here to find a list of Rifampicin & EEP suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Rifampicin & EEP Drug Master File in Japan (Rifampicin & EEP JDMF) empowers Rifampicin & EEP 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 Rifampicin & EEP JDMF during the approval evaluation for pharmaceutical products. At the time of Rifampicin & EEP 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 Rifampicin & EEP suppliers with JDMF on PharmaCompass.
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