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