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A limited number of biomedical procedures are used in human participant studies on the Ithaca campus...
Avoid delays by understanding the IRB process from protocol submission to review, revision, and appr...
The Cornell University Office of Research Integrity and Assurance (ORIA) and WCM Office of Research ...
Published on: Tuesday, July 30, 2019 - 3:04pm
IRB regulations now incorporate the broad definition of “clinical trial” adopted by the National Ins...
Research with human participants in other countries must comply with both U.S. and international eth...
When Cornell researchers plan to participate in a collaborative or multi-site study, there are a few...
Here you will find answers to frequently asked questions about human participant research at Cornell...
Revisions to the Federal policy for the protection of human participants in research (the "Common Ru...
Published on: Monday, June 10, 2019 - 10:22am
Learn about the research implications of the General Data Protection Regulation (GDPR).
Published on: Friday, June 14, 2019 - 3:51pm