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