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