01 1Cambrex Profarmaco Milano S. r. l.
02 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 2Diazepam
01 1Italy
02 1U.S.A
Registration Number : 218MF10146
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2006-01-31
Latest Date of Registration : 2018-12-11
Registration Number : 217MF10542
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2022-12-23
A Diazepam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diazepam, including repackagers and relabelers. The FDA regulates Diazepam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diazepam 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 Diazepam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diazepam supplier is an individual or a company that provides Diazepam active pharmaceutical ingredient (API) or Diazepam finished formulations upon request. The Diazepam suppliers may include Diazepam API manufacturers, exporters, distributors and traders.
click here to find a list of Diazepam 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 Diazepam Drug Master File in Japan (Diazepam JDMF) empowers Diazepam 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 Diazepam JDMF during the approval evaluation for pharmaceutical products. At the time of Diazepam 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 Diazepam suppliers with JDMF on PharmaCompass.
We have 2 companies offering Diazepam
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
