Consultation paper: Informed consent in the clinical trials regulation

We want your opinion! The EPF Secretariat has drafted a consultation paper (below), looking specifically at the information and informed consent aspects of the clinical trials regulation.

This document is largely based on our previous position papers.

Send us your comments!

Please send us your feedback to policy@eu-patient.eu by 18 March 2016.

Next steps

A revised version will be circulated for a second, shorter round of final comments.