Drug Master File
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Drug Master File or DMF is a document prepared by a pharmaceutical manufacturer and submitted solely at its discretion to the appropriate regulatory authority in the intended drug market. There is no regulatory requirement to file a DMF. Wikipedia
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Nov 3, 2023 · Drug master files (DMFs) are submissions to FDA used to provide confidential, detailed information about facilities, processes, or articles used ...
Mar 11, 2005 · A Drug Master File (DMF) is a submission to the Food and Drug Administration (FDA) that may be used to provide confidential detailed information ...
Drug Master File or DMF is a document prepared by a pharmaceutical manufacturer and submitted solely at its discretion to the appropriate regulatory ...