Guest Blog: Stephen Lock, Interim Chief Information and Technology Officer, NIHR CRN

The UK Health Data Research Alliance Board agreed to move beyond the ‘Green Paper’ phase of the Trusted Research Environment (TRE) programme at its meeting on 23 July 2020.  We are now pleased to publish our updated paper which is the result of a collaborative community effort. There was agreement in the concept and...

Three new members have joined the UK Health Data Research Alliance, a consortium of leading health data custodians and research organisations, working to accelerate the use of health data to improve health and care across the country. Thirty-three organisations in total have now joined the Alliance in the 18 months since its...

Data Safe Havens are an essential way of managing risk of unauthorised re-identification of individuals from de-identified data. This risk heightens with increased data linkage across a wider range of data sets. To date, most of the focus of Data Safe Havens has been on the people, processes and technology required to...

Three new members have joined the UK Health Data Research Alliance to support its goal of accelerating the use of health data to improve health and care across the UK. The new members will enrich and expand the range of datasets discoverable through the Innovation Gateway. This will include the Neonatal Data Analysis Unit at...

The inaugural UK Health Data Research Alliance Symposium took place in London on 4th February 2020. The event brought together more than 150 people working across the UK Health Data Research Alliance, Health Data Research Hubs, Innovation Gateway, Sandbox and others working closely with HDR UK on infrastructure.

Nine more health care and research organisations have signed up to join the UK Health Data Research Alliance to accelerate health discoveries using data in research. This boosts the Alliance membership to a total of 27 members – with over 400 datasets – each committing to make its data accessible for responsible research...

In order to reach our aim of maximising value of health data for research, it is important that as a community working across sectors that we are aligning around consistent standards for data to improve quality, interoperability, reuse, and translation to clinical care.

This month sees the initial launch of The Brain Tumour Charity’s ‘Brain tumouR Information and Analysis Network' or BRIAN for short.