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