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