Webinar: Congenital Anomaly Registration – December 2020
The NDRS Webinar on Congenital Anomaly Registration took place live on Wednesday 9th December.
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 explored:
- The NCARDRS path to national congenital anomaly data.
- The value and impact of congenital anomaly registration.
You can access the recording of the webinar here.
You can access the presentation slides from the webinar here:
Presentation 1 – Jenny Broughan – NCARDRS
Presentation 2 – Judith Rankin – Newcastle University
To contact the Congenital Anomalies team directly, you can email: firstname.lastname@example.org