A (2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol DMF (Drug Master File) is a document detailing the whole manufacturing process of (2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol active pharmaceutical ingredient (API) in detail. Different forms of (2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol DMFs exist exist since differing nations have different regulations, such as (2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A (2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol DMF submitted to regulatory agencies in the US is known as a USDMF. (2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol USDMF includes data on (2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The (2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol USDMF is kept confidential to protect the manufacturer’s intellectual property.
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