Participant’s Bill of Rights

Participants have the right to information about clinical research that they understand.

The Participants Bill of Rights* has been developed especially for people who want to learn more about what to expect when deciding whether to join a clinical research study.

This presentation can be used by researchers and other clinical research stakeholders to support efforts to raise awareness and educate their target audience about research

*This material was adapted from pamphlets developed by the New England Research Subject Advocacy Group, with contributions from the affiliated universities and academic healthcare centers of member institutions. For more information see: