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