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EUROAPI, the leading small molecules API player, provides both API sales & CDMO services. 
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01 EUROAPI ITALY S. r. l. (1)
01 Rifampicin (1)
01 France (1)
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PharmaCompass offers a list of Rifampin 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 Rifampin manufacturer or Rifampin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rifampin manufacturer or Rifampin supplier.
PharmaCompass also assists you with knowing the Rifampin API Price utilized in the formulation of products. Rifampin API Price is not always fixed or binding as the Rifampin Price is obtained through a variety of data sources. The Rifampin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rifampicin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rifampicin, including repackagers and relabelers. The FDA regulates Rifampicin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 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 Rifampicin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rifampicin supplier is an individual or a company that provides Rifampicin active pharmaceutical ingredient (API) or Rifampicin finished formulations upon request. The Rifampicin suppliers may include Rifampicin API manufacturers, exporters, distributors and traders.
click here to find a list of Rifampicin 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 Rifampicin Drug Master File in Japan (Rifampicin JDMF) empowers 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 Rifampicin JDMF during the approval evaluation for pharmaceutical products. At the time of 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 Rifampicin suppliers with JDMF on PharmaCompass.
