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