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