A (R)-5-((S)-1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one DMF (Drug Master File) is a document detailing the whole manufacturing process of (R)-5-((S)-1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one active pharmaceutical ingredient (API) in detail. Different forms of (R)-5-((S)-1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one DMFs exist exist since differing nations have different regulations, such as (R)-5-((S)-1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A (R)-5-((S)-1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one DMF submitted to regulatory agencies in the US is known as a USDMF. (R)-5-((S)-1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one USDMF includes data on (R)-5-((S)-1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The (R)-5-((S)-1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of (R)-5-((S)-1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one suppliers with USDMF on PharmaCompass.