Returning Study Results to Research Participants: Best Practices for Preparation and Institutional Review Board Oversight

By WIRB-Copernicus Group
Published: January 2019

Read this white paper, co-authored by the Center for Information and Study of Clinical Research Participation (CISCRP) to learn about the current best practices for the content and preparation of plain language summaries, and the current guidance for how sponsors should work with Institutional Review Boards (IRBs) which have oversight of the clinical trials for which the summaries are provided.

To learn more, register for our free white paper Returning Study Results to Research Participants: Best Practices for Preparation and Institutional Review Board Oversight.

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