This post was written by 67Health in partnership with Data Saves Lives. 67Health is a healthcare communications agency. Data Saves Lives is a multi-stakeholder initiative with the aim of […]
This post was written by 67Health in partnership with Data Saves Lives. 67Health is a healthcare communications agency. Data Saves Lives is a multi-stakeholder initiative with […]
This post was written by Dr Jessica Barnes, psychologist/behavioural scientist and qualitative researcher in the Cancer Behavioural Science Group at King’s College London. She is […]
Just over two years ago, on the 25th of May 2018, the UK government implemented the Data Protection Act across the country. This was the latest […]
In this series, members of our group, the wider research field & individuals from public interest groups will debate the use of patient data in […]
Is it ethical to enrol patients into a clinical trial without first obtaining their consent? Most people’s immediate reaction is “No”. But what should people […]
Is random fair? On the one hand, we feel than random selection is the fairest way to do things. Which side gets to choose whether […]
On 25th of May 2018 the EU General Data Protection Regulation (GDPR) went live. GDPR is designed to protect EU citizens from organisations using their data […]
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