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 : 2022-11-30
A Rifampin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rifampin, including repackagers and relabelers. The FDA regulates Rifampin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rifampin 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 Rifampin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rifampin supplier is an individual or a company that provides Rifampin active pharmaceutical ingredient (API) or Rifampin finished formulations upon request. The Rifampin suppliers may include Rifampin API manufacturers, exporters, distributors and traders.
click here to find a list of Rifampin 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 Rifampin Drug Master File in Japan (Rifampin JDMF) empowers Rifampin 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 Rifampin JDMF during the approval evaluation for pharmaceutical products. At the time of Rifampin 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 Rifampin suppliers with JDMF on PharmaCompass.
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