Links
Amendments to the HRRs
Artificial Intelligence
Audit and Service Evaluation
Broad Consent - is it permissible?
Case Reports / Case Studies / Case Series
Challenges in identifying Data Controllers
Copy of the Consent under the HRRs (as amended)
Cover under the Clinical Indemnity Scheme
DPIA and TIA for Research and Clinical Trials
DPIA / Data Protection Reviews
Health Research Data Protection Network
Health Research Regulations, Capacity and the HRCDC
Genetic Data - can it be anonymised?
Genomic Research
Public Patient Involvement (PPI)
NREC COVID-19
NREC-CT
NREC-MD
Radiation Questions
Radiation Studies
Research Database
Retrospective Chart Review Studies
RCSI Hospital Group - Research Ethics Committees
Site Sign Off Process
State Indemnity Guidance 10
Staff Survey Studies
The Irish Take - GDPR and Research
Third Parties and Contracts
Training #1- How to complete a REC Application
(40 mins)(Dr. Lyndon Walker)(2021)
Training #2- GDPR and Health Data
(35 mins)(plus 30 mins Q and A)(Ghent University DPO)(2021)
Training #3- Health Research Regulations 2018
(30 mins)(HRB)(2018)
Training #4- Submitting to Beaumont Hospital Research Ethics Committee
(5 mins)(video series)(Beaumont Ethics)(2024)
Training #5- Completing the Application Form and DPIA, and Developing Information Leaflets and Consent Forms
(instruction sheets and sample applications)(Beaumont Ethics)(2024)