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, Price,and more, enabling you to easily find the right Bromazepam manufacturer or Bromazepam supplier for your needs.
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PharmaCompass also assists you with knowing the Bromazepam API Price utilized in the formulation of products. Bromazepam API Price is not always fixed or binding as the Bromazepam Price is obtained through a variety of data sources. The Bromazepam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bromazepam ratiopharm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bromazepam ratiopharm, including repackagers and relabelers. The FDA regulates Bromazepam ratiopharm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bromazepam ratiopharm API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Bromazepam ratiopharm supplier is an individual or a company that provides Bromazepam ratiopharm active pharmaceutical ingredient (API) or Bromazepam ratiopharm finished formulations upon request. The Bromazepam ratiopharm suppliers may include Bromazepam ratiopharm API manufacturers, exporters, distributors and traders.
click here to find a list of Bromazepam ratiopharm 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 ratiopharm Drug Master File in Japan (Bromazepam ratiopharm JDMF) empowers Bromazepam ratiopharm 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 ratiopharm JDMF during the approval evaluation for pharmaceutical products. At the time of Bromazepam ratiopharm 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 ratiopharm suppliers with JDMF on PharmaCompass.
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