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?