01 1Cambrex Profarmaco Milano S. r. l.
01 1Medazepam
01 1U.S.A
Registration Number : 219MF10284
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2007-09-10
Latest Date of Registration : 2016-03-02
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PharmaCompass offers a list of Medazepam 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 Medazepam manufacturer or Medazepam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Medazepam manufacturer or Medazepam supplier.
A Medazepamum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Medazepamum, including repackagers and relabelers. The FDA regulates Medazepamum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Medazepamum 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 Medazepamum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Medazepamum supplier is an individual or a company that provides Medazepamum active pharmaceutical ingredient (API) or Medazepamum finished formulations upon request. The Medazepamum suppliers may include Medazepamum API manufacturers, exporters, distributors and traders.
click here to find a list of Medazepamum 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 Medazepamum Drug Master File in Japan (Medazepamum JDMF) empowers Medazepamum 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 Medazepamum JDMF during the approval evaluation for pharmaceutical products. At the time of Medazepamum 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 Medazepamum suppliers with JDMF on PharmaCompass.
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