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
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PharmaCompass offers a list of Diazepam 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 Diazepam manufacturer or Diazepam supplier for your needs.
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A Nerozen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nerozen, including repackagers and relabelers. The FDA regulates Nerozen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nerozen 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 Nerozen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Nerozen supplier is an individual or a company that provides Nerozen active pharmaceutical ingredient (API) or Nerozen finished formulations upon request. The Nerozen suppliers may include Nerozen API manufacturers, exporters, distributors and traders.
click here to find a list of Nerozen 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 Nerozen Drug Master File in Japan (Nerozen JDMF) empowers Nerozen 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 Nerozen JDMF during the approval evaluation for pharmaceutical products. At the time of Nerozen JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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