enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. MedCalc - Wikipedia

    en.wikipedia.org/wiki/MedCalc

    [2] [3] [4] It has an integrated spreadsheet for data input and can import files in several formats (Excel, SPSS, CSV, ...). MedCalc includes basic parametric and non-parametric statistical procedures and graphs such as descriptive statistics , ANOVA , Mann–Whitney test , Wilcoxon test , χ 2 test , correlation , linear as well as non-linear ...

  3. Clinical data repository - Wikipedia

    en.wikipedia.org/wiki/Clinical_data_repository

    A Clinical Data Repository (CDR) or Clinical Data Warehouse (CDW) is a real time database that consolidates data from a variety of clinical sources to present a unified view of a single patient. It is optimized to allow clinicians to retrieve data for a single patient rather than to identify a population of patients with common characteristics ...

  4. Clinical data management - Wikipedia

    en.wikipedia.org/wiki/Clinical_data_management

    The data management plan describes the activities to be conducted in the course of processing data. Key topics to cover include the SOPs to be followed, the clinical data management system (CDMS) to be used, description of data sources, data handling processes, data transfer formats and process, and quality control procedure

  5. 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. Systems for ...

  6. Case report form - Wikipedia

    en.wikipedia.org/wiki/Case_report_form

    All data on each patient participating in a clinical trial are held and/or documented in the CRF, including adverse events. The sponsor of the clinical trial develops the CRF to collect the specific data they need in order to test their hypotheses or answer their research questions. The size of a CRF can range from a handwritten one-time ...

  7. Clinical data acquisition - Wikipedia

    en.wikipedia.org/wiki/Clinical_data_acquisition

    Acquisition or collection of clinical trial data can be achieved through various methods that may include, but are not limited to, any of the following: paper or electronic medical records, paper forms completed at a site, interactive voice response systems, local electronic data capture systems, or central web based systems.

  8. List of statistical software - Wikipedia

    en.wikipedia.org/wiki/List_of_statistical_software

    Orange, a data mining, machine learning, and bioinformatics software; Pandas – High-performance computing (HPC) data structures and data analysis tools for Python in Python and Cython (statsmodels, scikit-learn) Perl Data Language – Scientific computing with Perl; Ploticus – software for generating a variety of graphs from raw data

  9. Clinical data standards - Wikipedia

    en.wikipedia.org/wiki/Clinical_data_standards

    Clinical data standards are used to store and communicate information related to healthcare so that its meaning is unambiguous. They are used in clinical practice, in activity analysis and finding, and in research and development. There are many existing and proposed standards and many bodies working in this field.