Events2018-03-29T14:41:36+02:00

Events

“Better Science, Better Health” hosts a series of international conferences to outline research and innovation in adaptive clinical pathways and patient data usage.

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Digital Health: Catapulting Personalised Medicine Forward

November 27th, 2014 - Connected Digital Economy Catapult, London This round table will feature demonstrations of how next-generation technologies and social media will integrate with public health, thus facilitating the burgeoning market for personalised medicines. The session will include disruptive start-ups and technology savvy practitioners finding common ground in the desire to bring stratified medicines to patients. This event is organised in collaboration with: *

Enabling technologies for better patient outcomes – Live streaming from the European Health Forum Gastein

Streamed from the European Health Forum Gastein on October 1st, 2014, 9.00 - 11.00 CET

This session brings together industry, policy-makers and international experts on emerging technologies that harness the use of real world data to improve patient outcomes and accelerate clinical development. We will highlight the opportunity provided by robust data analysis and outline the current patient data activities in the EU 28 Member States.

Real World Evidence in Adaptive Clinical Trial Design

September 17th, 2014, Brussels, 9.00-14.00 CET

What does Europe need to do to make this technology stew of mobile apps, eHealth platforms, and national heatlhcare systems work together in seamless harmony?

This round table is organised in partnership with:
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Sustainable health systems for inclusive growth in Europe

19-20 November, Vilnius: The main aim of the annual Conference, which will be held under the auspices of the Lithuanian Presidency of the Council of the EU, is to identify the existing best evidence on fostering the development of sustainable health systems throughout the entire Europe.

A Roadmap for Sharing Clinical Trial Data

August 27th, 2013 Brussels

EFPIA and the Pharmaceutical Research and Manufacturers of America (PhRMA) have issued a joint proposal to enhance responsible clinical trial data sharing. What does this mean practically for research in Europe, and what are the best practices for implementation?

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