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