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