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