01 1Siegfried Evionnaz SA
01 1Ribavirin Ribavirin
01 1Switzerland
Registration Number : 221MF10051
Registrant's Address : Route du Simplon 1,36,CH-1902 Evionnaz,Switzerland
Initial Date of Registration : 2009-03-09
Latest Date of Registration : 2009-03-09
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PharmaCompass offers a list of Ribavirin 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 Ribavirin manufacturer or Ribavirin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ribavirin manufacturer or Ribavirin supplier.
PharmaCompass also assists you with knowing the Ribavirin API Price utilized in the formulation of products. Ribavirin API Price is not always fixed or binding as the Ribavirin Price is obtained through a variety of data sources. The Ribavirin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vilona manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vilona, including repackagers and relabelers. The FDA regulates Vilona manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vilona 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 Vilona manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vilona supplier is an individual or a company that provides Vilona active pharmaceutical ingredient (API) or Vilona finished formulations upon request. The Vilona suppliers may include Vilona API manufacturers, exporters, distributors and traders.
click here to find a list of Vilona 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 Vilona Drug Master File in Japan (Vilona JDMF) empowers Vilona 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 Vilona JDMF during the approval evaluation for pharmaceutical products. At the time of Vilona 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 Vilona suppliers with JDMF on PharmaCompass.
