drug master file

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Drug Master File or DMF is a document prepared by a manufacturer in the pharmaceutical industry and submitted solely at his discretion to the Food and Drug Administration (FDA). There is no requirement by law or FDA regulation to present a DMF. The document 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
drug master file

    Heceleme

    drug mas·ter file

    Türkçe nasıl söylenir

    drʌg mästır fayl

    Telaffuz

    /ˈdrəg ˈmastər ˈfīl/ /ˈdrʌɡ ˈmæstɜr ˈfaɪl/