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  2. JANUS clinical trial data repository - Wikipedia

    en.wikipedia.org/wiki/JANUS_clinical_trial_data...

    Janus clinical trial data repository is a clinical trial data repository (or data warehouse) standard as sanctioned by the U.S. Food and Drug Administration (FDA). It was named for the Roman god Janus (mythology), who had two faces, one that could see in the past and one that could see in the future.

  3. Quality by design - Wikipedia

    en.wikipedia.org/wiki/Quality_by_design

    Quality by design (QbD) is a concept first outlined by quality expert Joseph M. Juran in publications, most notably Juran on Quality by Design. [1] Designing for quality and innovation is one of the three universal processes of the Juran Trilogy, in which Juran describes what is required to achieve breakthroughs in new products, services, and processes. [2]

  4. Template:Infobox drug/doc/FDA-2023 - Wikipedia

    en.wikipedia.org/wiki/Template:Infobox_drug/doc/...

    * Drugs@FDA includes information about drugs, including biological products, approved for human use in the United States (see FAQ), but does not include information about FDA-approved products regulated by the Center for Biologics Evaluation and Research (for example, vaccines, allergenic products, blood and blood products, plasma derivatives, cellular and gene therapy products).

  5. Investigator's brochure - Wikipedia

    en.wikipedia.org/wiki/Investigator's_brochure

    Owing to the importance of the IB in maintaining the safety of human subjects in clinical trials, and as part of their guidance on good clinical practice (GCP), the U.S. Food and Drug Administration (FDA) has written regulatory codes and guidances for authoring the IB, and the International Conference on Harmonisation (ICH) has prepared a ...

  6. CFR - Code of Federal Regulations Title 21

    highline.huffingtonpost.com/miracleindustry/...

    identification numbers of all drug master files and other applications under this part that are referenced in the application; and the drug product's proposed indications for use. (2) A statement whether the submission is an original submission, a 505(b)(2) application, a resubmission, or a supplement to an

  7. QBD - Wikipedia

    en.wikipedia.org/wiki/QBD

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  8. Electronic common technical document - Wikipedia

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

    This is the file index.xml in the submission sequence number folder. For example: ctd-123456/0000/index.xml The purpose of this file is twofold: Manage meta-data for the entire submission; Constitute a comprehensive table of contents and provide corresponding navigation aid.

  9. Trial master file - Wikipedia

    en.wikipedia.org/wiki/Trial_master_file

    Different file systems have different limits on the depth of the filename path, creating potential problems and limitations based on the file system hierarchy in use. [10] Thirdly, with respect to the use of the TMF Reference Model as a database schema, the TMF RM v3.0 spreadsheet cannot be used without manual modification as a classification ...

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