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