A Genesa DMF (Drug Master File) is a document detailing the whole manufacturing process of Genesa active pharmaceutical ingredient (API) in detail. Different forms of Genesa DMFs exist exist since differing nations have different regulations, such as Genesa USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Genesa DMF submitted to regulatory agencies in the US is known as a USDMF. Genesa USDMF includes data on Genesa's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Genesa USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Genesa suppliers with USDMF on PharmaCompass.