01 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 1Nitrazepam
01 1Italy
Registration Number : 217MF10544
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2018-07-03
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PharmaCompass offers a list of Nitrazepam 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 Nitrazepam manufacturer or Nitrazepam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nitrazepam manufacturer or Nitrazepam supplier.
PharmaCompass also assists you with knowing the Nitrazepam API Price utilized in the formulation of products. Nitrazepam API Price is not always fixed or binding as the Nitrazepam Price is obtained through a variety of data sources. The Nitrazepam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Somnibel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Somnibel, including repackagers and relabelers. The FDA regulates Somnibel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Somnibel 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 Somnibel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Somnibel supplier is an individual or a company that provides Somnibel active pharmaceutical ingredient (API) or Somnibel finished formulations upon request. The Somnibel suppliers may include Somnibel API manufacturers, exporters, distributors and traders.
click here to find a list of Somnibel 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 Somnibel Drug Master File in Japan (Somnibel JDMF) empowers Somnibel 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 Somnibel JDMF during the approval evaluation for pharmaceutical products. At the time of Somnibel 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 Somnibel suppliers with JDMF on PharmaCompass.
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