01 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 1Clonazepam
01 1Italy
Registration Number : 217MF10543
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2010-03-17
A Clonazepam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clonazepam, including repackagers and relabelers. The FDA regulates Clonazepam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clonazepam 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 Clonazepam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clonazepam supplier is an individual or a company that provides Clonazepam active pharmaceutical ingredient (API) or Clonazepam finished formulations upon request. The Clonazepam suppliers may include Clonazepam API manufacturers, exporters, distributors and traders.
click here to find a list of Clonazepam 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 Clonazepam Drug Master File in Japan (Clonazepam JDMF) empowers Clonazepam 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 Clonazepam JDMF during the approval evaluation for pharmaceutical products. At the time of Clonazepam 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 Clonazepam suppliers with JDMF on PharmaCompass.
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