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Tenofovir Disoproxil Fumarate IP
Date of Issue : 2024-04-23
Valid Till : 2027-04-22
Written Confirmation Number : WC-0170
Address of the Firm : Plot No. 41, 42/2, 42/1/B, 43, 40, 59, 58 GIDC, Vapi, Dist: Valsad -396195, Guja...
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PharmaCompass offers a list of Tenofovir Disoproxil Fumarate 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 Disoproxil Fumarate manufacturer or Tenofovir Disoproxil Fumarate supplier for your needs.
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PharmaCompass also assists you with knowing the Tenofovir Disoproxil Fumarate API Price utilized in the formulation of products. Tenofovir Disoproxil Fumarate API Price is not always fixed or binding as the Tenofovir Disoproxil Fumarate Price is obtained through a variety of data sources. The Tenofovir Disoproxil Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tenofovir Disoproxil Fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenofovir Disoproxil Fumarate, including repackagers and relabelers. The FDA regulates Tenofovir Disoproxil Fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenofovir Disoproxil Fumarate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tenofovir Disoproxil Fumarate supplier is an individual or a company that provides Tenofovir Disoproxil Fumarate active pharmaceutical ingredient (API) or Tenofovir Disoproxil Fumarate finished formulations upon request. The Tenofovir Disoproxil Fumarate suppliers may include Tenofovir Disoproxil Fumarate API manufacturers, exporters, distributors and traders.
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A Tenofovir Disoproxil Fumarate written confirmation (Tenofovir Disoproxil Fumarate WC) is an official document issued by a regulatory agency to a Tenofovir Disoproxil Fumarate manufacturer, verifying that the manufacturing facility of a Tenofovir Disoproxil Fumarate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tenofovir Disoproxil Fumarate APIs or Tenofovir Disoproxil Fumarate finished pharmaceutical products to another nation, regulatory agencies frequently require a Tenofovir Disoproxil Fumarate WC (written confirmation) as part of the regulatory process.
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We have 16 companies offering Tenofovir Disoproxil Fumarate
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