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