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