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