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