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