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  2. Clinical data management - Wikipedia

    en.wikipedia.org/wiki/Clinical_data_management

    Clinical data management (CDM) is a critical process in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials. [1] Clinical data management ensures collection, integration and availability of data at appropriate quality and cost.

  3. Clinical data management system - Wikipedia

    en.wikipedia.org/wiki/Clinical_data_management...

    A clinical data management system or CDMS is a tool used in clinical research to manage the data of a clinical trial. The clinical trial data gathered at the investigator site in the case report form are stored in the CDMS. To reduce the possibility of errors due to human entry, the systems employ various means to verify the data.

  4. Data clarification form - Wikipedia

    en.wikipedia.org/wiki/Data_clarification_form

    A data clarification form (DCF) [1] or data query form is a questionnaire specifically used in clinical research. The DCF is the primary data clarification tool from the trial sponsor or contract research organization (CRO) towards the investigator to clarify discrepancies and ask the investigator for clarification. The DCF is part of the data ...

  5. Good clinical data management practice - Wikipedia

    en.wikipedia.org/wiki/Good_Clinical_Data...

    Good clinical data management practice (GCDMP) is the current industry standards for clinical data management that consist of best business practice and acceptable regulatory standards. In all phases of clinical trials , clinical and laboratory information must be collected and converted to digital form for analysis and reporting purposes.

  6. Fast Healthcare Interoperability Resources - Wikipedia

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

    The Fast Healthcare Interoperability Resources (FHIR, / f aɪər /, like fire) standard is a set of rules and specifications for the secure exchange of electronic health care data. It is designed to be flexible and adaptable, so that it can be used in a wide range of settings and with different health care information systems.

  7. 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.

  8. Eggs now qualify as ‘healthy’ food, FDA says: Here’s why

    www.aol.com/eggs-now-qualify-healthy-food...

    The U.S. Food and Drug Administration (FDA) now classifies eggs as a “healthy, nutrient-dense" food, according to a new proposed rule. Registered dietitians react to the change.

  9. Observational Health Data Sciences and Informatics - Wikipedia

    en.wikipedia.org/wiki/Observational_Health_Data...

    [3] [4] OMOP developed a Common Data Model (CDM), standardizing the way observational data is represented. [3] After OMOP ended, this standard started being maintained and updated by OHDSI. [1] As of February 2024, the most recent CDM is at version 6.0, while version 5.4 is the stable version used by most tools in the OMOP ecosystem. [5]