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