A 0791, MK DMF (Drug Master File) is a document detailing the whole manufacturing process of 0791, MK active pharmaceutical ingredient (API) in detail. Different forms of 0791, MK DMFs exist exist since differing nations have different regulations, such as 0791, MK USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 0791, MK DMF submitted to regulatory agencies in the US is known as a USDMF. 0791, MK USDMF includes data on 0791, MK's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 0791, MK USDMF is kept confidential to protect the manufacturer’s intellectual property.
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