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