Research Data Scotland (RDS) provide a simple explanation of how data is de-identified, what is meant by the term anonymisation and how this differs from pseudonymisation.

This Health Data Research UK bite-sized video covers strategies to build trust and engage underserved communities in data-enabled clinical trials. You will discover how partnerships, co-design and addressing barriers to participation can foster inclusivity and improve diversity in trial participation.

This PEDRI (Public Engagement in Data Research) webinar introduces using Equality Impact Assessments to embed equitable, inclusive public involvement in data research.