01 1Gilead Alberta ULC
01 1Tenofovir Ara Fe Nami de fumarate
01 1U.S.A
Tenofovir alafenamide fumarate
Registration Number : 227MF10232
Registrant's Address : 1021 Hayter Road Edmonton, Alberta T6S 1A1, Canada
Initial Date of Registration : 2015-09-24
Latest Date of Registration : 2021-12-22
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PharmaCompass offers a list of Tenofovir 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 Tenofovir manufacturer or Tenofovir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tenofovir manufacturer or Tenofovir supplier.
PharmaCompass also assists you with knowing the Tenofovir API Price utilized in the formulation of products. Tenofovir API Price is not always fixed or binding as the Tenofovir Price is obtained through a variety of data sources. The Tenofovir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tenefovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenefovir, including repackagers and relabelers. The FDA regulates Tenefovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenefovir 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 Tenefovir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tenefovir supplier is an individual or a company that provides Tenefovir active pharmaceutical ingredient (API) or Tenefovir finished formulations upon request. The Tenefovir suppliers may include Tenefovir API manufacturers, exporters, distributors and traders.
click here to find a list of Tenefovir 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 Tenefovir Drug Master File in Japan (Tenefovir JDMF) empowers Tenefovir 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 Tenefovir JDMF during the approval evaluation for pharmaceutical products. At the time of Tenefovir 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 Tenefovir suppliers with JDMF on PharmaCompass.
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