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You are here:
  1. European CommissionEU Science Hub
  2. European Platform on Rare Disease Registration
  3. EUROCAT

Data Collection

  • Guidelines for data registration

    Guidelines for data registration

    Detailed EUROCAT guidelines for data collection, coding and classification of congenital anomalies and data transmission to the Central Registry.

     
  • Data management program (EDMP)

    Data Management Software (DMS)

    Detailed description of the EUROCAT Data Management Software (DMS) for database management, data validation, reporting of prevalence and statistical monitoring of congenital anomalies.

     
  • Data Quality

    Data Quality

    Data Quality Indicators (DQIs) assess five fey elements of data quality: completeness of case ascertainment, accuracy of diagnosis, completeness of information on EUROCAT variables, timeliness of data transmission and availability of population denominator information.

     
  • Requesting EUROCAT data

    Requesting EUROCAT data

    EUROCAT encourages the use of its data for epidemiological surveillance and research. Read more about the conditions and procedures to request data.

     
  • Exchange portal

    Data Exchange Portal

    Access to the Data Exchange Portal (for authorised EUROCAT members only).

     

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