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