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