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
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PharmaCompass offers a list of Clonazepam 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 Clonazepam manufacturer or Clonazepam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clonazepam manufacturer or Clonazepam supplier.
PharmaCompass also assists you with knowing the Clonazepam API Price utilized in the formulation of products. Clonazepam API Price is not always fixed or binding as the Clonazepam Price is obtained through a variety of data sources. The Clonazepam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Iktorivil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iktorivil, including repackagers and relabelers. The FDA regulates Iktorivil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iktorivil 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 Iktorivil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Iktorivil supplier is an individual or a company that provides Iktorivil active pharmaceutical ingredient (API) or Iktorivil finished formulations upon request. The Iktorivil suppliers may include Iktorivil API manufacturers, exporters, distributors and traders.
click here to find a list of Iktorivil 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 Iktorivil Drug Master File in Japan (Iktorivil JDMF) empowers Iktorivil 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 Iktorivil JDMF during the approval evaluation for pharmaceutical products. At the time of Iktorivil 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 Iktorivil suppliers with JDMF on PharmaCompass.
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