DMF Fda Abbreviation

DMF has various meanings in the Fda category. Discover the full forms, definitions, and usage contexts of DMF in Fda.

Drug Master File

Most Common

A Drug Master File (DMF) is a submission to the Food and Drug Administration (FDA) that may be used to provide confidential detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of one or more human drugs.

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