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  2. Drug Master File - Wikipedia

    en.wikipedia.org/wiki/Drug_Master_File

    In the United States, DMFs are submitted to the Food and Drug Administration (FDA). The Main Objective of the DMF is to support regulatory requirements and to prove the quality, safety and efficacy of the medicinal product for obtaining an Investigational New Drug Application (IND), a New Drug Application (NDA),As an Abbreviated New Drug Application (ANDA), another DMF, or an Export Application.

  3. Dimethyl fumarate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_fumarate

    Dimethyl fumarate (DMF) is the methyl ester of fumaric acid and is named after the earth smoke plant (Fumaria officinalis). [8] Dimethyl fumarate combined with three other fumaric acid esters (FAEs) is solely licensed in Germany as an oral therapy for psoriasis (brand name Fumaderm ). [ 9 ]

  4. Dimethylformamide - Wikipedia

    en.wikipedia.org/wiki/Dimethylformamide

    Dimethylformamide is an organic compound with the chemical formula H C O N (CH3)2. Its structure is HC (=O)−N (−CH 3)2. Commonly abbreviated as DMF (although this initialism is sometimes used for dimethylfuran, or dimethyl fumarate), this colourless liquid is miscible with water and the majority of organic liquids.

  5. Electronic common technical document - Wikipedia

    en.wikipedia.org/wiki/Electronic_Common...

    The electronic common technical document (eCTD) is an interface and international specification for the pharmaceutical industry to agency transfer of regulatory information. The specification is based on the Common Technical Document (CTD) format and was developed by the International Council for Harmonisation (ICH) Multidisciplinary Group 2 ...

  6. Common Technical Document - Wikipedia

    en.wikipedia.org/wiki/Common_Technical_Document

    The CTD is an internationally agreed format for the preparation of applications regarding new drugs intended to be submitted to regional regulatory authorities in participating countries. It was developed by the European Medicines Agency (EMA, Europe), the Food and Drug Administration and the Ministry of Health, Labour and Welfare (Japan ...

  7. Gilead gets US FDA approval for inflammatory liver disease drug

    www.aol.com/news/us-fda-approves-gileads-liver...

    By Puyaan Singh and Leroy Leo. (Reuters) -The U.S. Food and Drug Administration on Wednesday approved Gilead Sciences' liver disease treatment, Livdelzi, which it gained through a $4.3 billion ...

  8. Dextromethorphan - Wikipedia

    en.wikipedia.org/wiki/Dextromethorphan

    Dextromethorphan is the dextrorotatory enantiomer of levomethorphan, which is the methyl ether of levorphanol, both opioid analgesics. It is named according to IUPAC rules as (+)-3-methoxy-17-methyl-9α,13α,14α- morphinan. As its pure form, dextromethorphan occurs as an odorless, opalescent white powder.

  9. DMF - Wikipedia

    en.wikipedia.org/wiki/DMF

    DMF may refer to: Science and technology ... Drug Master File, a document in the pharmaceutical industry; Other technology. Digital microfluidics, ...