5:30pm-7:00pm on Thursday 14 March
online, online, online
Research using data from patient records has the potential to increase our understanding of health conditions and support the development of better treatments and medicines.
Most of the health data that is used in research has identifying information removed from it to increase privacy and security, and a variety of opt-in or opt-out options are available to support patient choice – but what impact do these measures have on the quality, equity and possibilities of the research?
Join our expert panel as they discuss how different choices around data influence outcomes for the research, for patients and for the NHS