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