Find a compilation of all the workshop panels here:


Informed consent in the digital era: Is technology a silver bullet? Ethics and data protection considerations


Session 1 – Perspectives on the future of consent in clinical research


Consent solutions for secondary use of trial data after the end of the trial


The implications of big data for informed consent


Session 2 – The EU regulatory landscape for consent in clinical research


Informed consent – Council of Europe reference work and new challenges


Does the EDPB forces us to come up with another legal ground under GDPR for clinical trials?