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