01 1Cambrex Profarmaco Milano S. r. l.
02 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 2Diazepam
01 1Italy
02 1U.S.A
Registration Number : 218MF10146
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2006-01-31
Latest Date of Registration : 2018-12-11
Registration Number : 217MF10542
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2022-12-23
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PharmaCompass offers a list of Diazepam 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 Diazepam manufacturer or Diazepam supplier for your needs.
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PharmaCompass also assists you with knowing the Diazepam API Price utilized in the formulation of products. Diazepam API Price is not always fixed or binding as the Diazepam Price is obtained through a variety of data sources. The Diazepam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BRN 0754371 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BRN 0754371, including repackagers and relabelers. The FDA regulates BRN 0754371 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BRN 0754371 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 BRN 0754371 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A BRN 0754371 supplier is an individual or a company that provides BRN 0754371 active pharmaceutical ingredient (API) or BRN 0754371 finished formulations upon request. The BRN 0754371 suppliers may include BRN 0754371 API manufacturers, exporters, distributors and traders.
click here to find a list of BRN 0754371 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 BRN 0754371 Drug Master File in Japan (BRN 0754371 JDMF) empowers BRN 0754371 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 BRN 0754371 JDMF during the approval evaluation for pharmaceutical products. At the time of BRN 0754371 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 BRN 0754371 suppliers with JDMF on PharmaCompass.
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