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 Roche Brand manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bromazepam Roche Brand, including repackagers and relabelers. The FDA regulates Bromazepam Roche Brand manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bromazepam Roche Brand 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 Roche Brand supplier is an individual or a company that provides Bromazepam Roche Brand active pharmaceutical ingredient (API) or Bromazepam Roche Brand finished formulations upon request. The Bromazepam Roche Brand suppliers may include Bromazepam Roche Brand API manufacturers, exporters, distributors and traders.
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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 Roche Brand Drug Master File in Japan (Bromazepam Roche Brand JDMF) empowers Bromazepam Roche Brand 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 Roche Brand JDMF during the approval evaluation for pharmaceutical products. At the time of Bromazepam Roche Brand 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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