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  2. Template:ClinicalStudyInfo/doc - Wikipedia

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

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Donate; Help; Learn to edit; Community portal; Recent changes; Upload file

  3. Case report form - Wikipedia

    en.wikipedia.org/wiki/Case_report_form

    A case report form (or CRF) is a paper or electronic questionnaire specifically used in clinical trial research. [1] The case report form is the tool used by the sponsor of the clinical trial to collect data from each participating patient.

  4. Clinical study report - Wikipedia

    en.wikipedia.org/wiki/Clinical_study_report

    In medicine, a clinical study report (CSR) on a clinical trial is a document, typically very long, providing much detail about the methods and results of a trial. A CSR is a scientific document addressing efficacy and safety, not a sales or marketing tool; its content is similar to that of a peer-reviewed academic paper. [ 1 ]

  5. Consolidated Clinical Document Architecture - Wikipedia

    en.wikipedia.org/wiki/Consolidated_Clinical...

    Progress Note - This template represents a patient's clinical status during a hospitalization, outpatient visit, treatment with a LTPAC provider, or other healthcare encounter. [ 14 ] Transfer Summary - The Transfer Summary standardizes critical information for exchange of information between providers of care when a patient moves between ...

  6. Case report - Wikipedia

    en.wikipedia.org/wiki/Case_report

    In medicine, a case report is a detailed report of the symptoms, signs, diagnosis, treatment, and follow-up of an individual patient. Case reports may contain a demographic profile of the patient, but usually describe an unusual or novel occurrence. Some case reports also contain a literature review of other reported cases.

  7. Trial master file - Wikipedia

    en.wikipedia.org/wiki/Trial_master_file

    Article 58 requires that "the sponsor and investigator shall archive the content of the clinical trial master file for at least 25 years after the end of the clinical trial." This requirement defines a minimum retention period across the EU for all clinical trial master files, irrespective of whether the data subsequently supports a marketing ...

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  9. Outcome measure - Wikipedia

    en.wikipedia.org/wiki/Outcome_measure

    Composite measures or combined measures are common in clinical research. [1] [2] The rationale is that combining different outcome measures gives greater statistical power. For example, the composite measure "Killed or Seriously Injured" is often used in studies of road safety. While deaths are easier to count and are an outcome of undisputed ...