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