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