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  2. Approved Drug Products with Therapeutic Equivalence ...

    en.wikipedia.org/wiki/Approved_Drug_Products...

    Therapeutic equivalence evaluations in this publication are not official FDA actions affecting the legal status of products under the Act. Finally, the Orange Book lists patents that are purported to protect each drug. Patent listings and use codes are provided by the drug application owner, and the FDA is obliged to list them.

  3. Electronic trial master file - Wikipedia

    en.wikipedia.org/wiki/Electronic_trial_master_file

    An electronic trial master file (eTMF) is a trial master file in electronic (digital content) format.It is a type of content management system for the pharmaceutical industry, providing a formalized means of organizing and storing documents, images, and other digital content for pharmaceutical clinical trials that may be required for compliance with government regulatory agencies.

  4. Office of Global Regulatory Operations and Policy - Wikipedia

    en.wikipedia.org/wiki/Office_of_Global...

    FDA Building 32 houses the Office of the Commissioner and the Office of Regulatory Affairs. The Office of Global Regulatory Operations and Policy (GO), [1] also known as the Office of Regulatory Affairs (ORA), [2] is the part of the U.S. Food and Drug Administration (FDA) enforcing the federal laws governing biologics, cosmetics, dietary supplements, drugs, food, medical devices, radiation ...

  5. Fast Healthcare Interoperability Resources - Wikipedia

    en.wikipedia.org/wiki/Fast_Healthcare...

    DSTU1 (First Draft Standard for Trial Use) official version published [5] [6] 2015-10-24: 1.0.2: DSTU2 (Second Draft Standard for Trial Use) official version published [5] 2019-10-24: 3.0.1: STU3 (Third Standard for Trial Use) [5] included coverage of a variety of clinical workflows, a Resource Description Framework format, and a variety of ...

  6. Abbreviated New Drug Application - Wikipedia

    en.wikipedia.org/wiki/Abbreviated_New_Drug...

    An Abbreviated New Drug Application (ANDA) is an application for a U.S. generic drug approval for an existing licensed medication or approved drug.. The ANDA is submitted to FDA's Center for Drug Evaluation and Research, Office of Generic Drugs, which provides for the review and ultimate approval of a generic drug product.

  7. OpenFDA - Wikipedia

    en.wikipedia.org/wiki/OpenFDA

    OpenFDA is a project indexing and formatting Food and Drug Administration (FDA) data, and making it accessible to the public. The ultimate goal of enabling the data accessibility is to educate people and save lives. The currently provided API of accessing data is under beta version. The project is open source and the code is available from GitHub.

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  9. Electronic common technical document - Wikipedia

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

    Version 2.0 of eCTD – an upgrade over the original CTD – was finalized on February 12, 2002, [1] and version 3.0 was finalized on October 8 of the same year. [2] As of August 2016, the most current version is 3.2.2, released on July 16, 2008. [3] A Draft Implementation Guide (DIG) for version 4.0 of eCTD was released in August 2012. [4]