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