Confused about the new national data opt-out (NDO) and how (if at all) it works with the GDPR? Johan Ordish untangles the web in the first of two blogs on the incoming opt-out process for health data
We are working with regulators, academics and developers to better understand the regulatory landscape that algorithms fit into in healthcare
Given the implications for patient safety and care, why isn't variant data systematically centralised?
NDG paper on data sharing for clinical genetics and genomics draws on NDG evidence session held in collaboration with PHG Foundation and the Association for Clinical Genomic Science (ACGS)
New recommendations for policy makers on improving the linkage and sharing of routine health data for research in England