Consent and patient information materials

NEW: A National Data Opt-Out is being introduced from March 2020 to enable patients to opt out from the use of their data for research or planning purposes. IBD Teams submitting data to the Registry should read our new guidance on what this means to ensure compliance with patient data preferences.

 https://ibdregistry.org.uk/wp-content/uploads/2020/02/IBD-Registry-patient-consent-and-the-National-data-opt-out-final-2020-02-20-1.pdf  (PDF 140KB)