A Gallium 67 citrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Gallium 67 citrate active pharmaceutical ingredient (API) in detail. Different forms of Gallium 67 citrate DMFs exist exist since differing nations have different regulations, such as Gallium 67 citrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Gallium 67 citrate DMF submitted to regulatory agencies in the US is known as a USDMF. Gallium 67 citrate USDMF includes data on Gallium 67 citrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Gallium 67 citrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
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