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NDRS Webinar: Congenital Anomaly Registration

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This webinar will give you an overview of NDRS’s work on congenital anomaly registration and analysis.

About this Event

This autumn the National Disease Registration Service (NDRS) is running a series of webinars to continue to share information about our latest work and developments. Each lunchtime webinar will focus on a different area of NDRS and there will be an opportunity to ask questions following the presentation.

The National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) forms part of NDRS and collects and analyses data on congenital anomalies and rare diseases.

This webinar on congenital anomalies will explore:

  • The NCARDRS path to national congenital anomaly data .
  • An overview of 2018 congenital anomaly data, the first year of national data.
  • NCARDRS’s work with the Fetal Anomaly Screening programme.
  • The value and impact of congenital anomaly registration.

Attendees will be sent joining instructions for the webinar 2 days beforehand. The webinar will be hosted on Microsoft Teams and will be accessible across desktop, browser and mobile (iOS or Android). Slides from presentations will be shared with attendees after the event.

If you have any questions about this webinar or registering to attend, please contact NDRSengagement@phe.gov.uk.

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