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