01 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 1Bromazepam
01 1Italy
Registration Number : 220MF10166
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2008-07-24
Latest Date of Registration : 2010-10-14
A Bromazepam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bromazepam, including repackagers and relabelers. The FDA regulates Bromazepam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bromazepam 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 Bromazepam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bromazepam supplier is an individual or a company that provides Bromazepam active pharmaceutical ingredient (API) or Bromazepam finished formulations upon request. The Bromazepam suppliers may include Bromazepam API manufacturers, exporters, distributors and traders.
click here to find a list of Bromazepam 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 Bromazepam Drug Master File in Japan (Bromazepam JDMF) empowers Bromazepam 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 Bromazepam JDMF during the approval evaluation for pharmaceutical products. At the time of Bromazepam 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 Bromazepam suppliers with JDMF on PharmaCompass.
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