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