Guidance for use of venipuncture for blood collection for research involving human participants.
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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...
This is an approved guidance document, detailing the role and responsibilities of Conflict Managers,...
The intent of this document is to describe the Post Approval Monitoring (PAM) program at Cornell Uni...
Geneva’s Discoveries to Commercialization
Join the Life Science Team at the Center for Technology Licensing (CTL) for an informational and int...
Cornell’s Individual Standard Non-Disclosure Agreement (NDA) is a mechanism by which a Cornell emplo...