IT TAKES MORE THAN JUST A REGISTRY TO IMPROVE CARE: HOW CAN WE USE DATA TO RAISE AWARENESS AND INITIATE ACTION TO IMPROVE OUTCOMES FOR PEOPLE WITH DIABETES?
Welcome and introduction David Matthews, University of Oxford, vice-chair EUDF
How can we use data to raise awareness and initiate action? Chaired by David Matthews
- Keynote – Developing missing targets: the diabetes treatment target – Bente Mikkelsen, Global Director NCD Department WHO
- Recommendations for implementation from EUDF – Robert Heine, chair EUDF Strategic Forum Data & Registries, Lilly
- Best practices – Using registries to improve quality of care and outcomes
- SWEET – Thomas Danne, Auf der Bult Hospital Hannover, SWEET Chairman & ISPAD Delegate Chairman
- The Swedish National Diabetes Register – Katerina Eeg-Olofsson, Sahlgrenska University Hospital, University of Gothenburg
- How to re-use health data for the benefit of public health, research and innovation? Andrzej Rys, Director Health systems, medical products and innovation DG Santé, European Commission
Panel discussion & questions from the audience chaired by Chantal Mathieu, University of Leuven, chair EUDF
- What’s in it for people with diabetes? Bastian Hauck, IDF Europe Board Member
- How to use feedback from registries in the clinical practice? Kamlesh Khunti, University of Leicester
- What are the opportunities for research? Jeannette Soderberg, Director European Research JDRF
- What is the perspective of the European Parliament? Tomislav Sokol, MEP, Member of the European Parliament Mobilizing for Diabetes
- What are the perspectives from industry? Maja Bujas-Bobanovic, EFPIA Diabetes platform, Sanofi
Closing remarks David Matthews
