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