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