Informed consent is more than just a form; it is a process that takes place between researcher and p...
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Whether you are working with an existing data set collected by another researcher, storing data you ...
This page contains information for researchers and research participants on how and when to report s...
Looking for guidance and resources? The links and documents below will help you to understand the ma...
Institutional Review Board for Human Participant Research (IRB) Office
Institutional Review Board for Human Participant Research (IRB) Office
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...
Cornell provides a secure registry system for faculty, staff, and students to record Cornell-related...
Guidance provided by the Cornell IRB for identifying and managing compliance for clinical trials inv...
Once your research project is complete, you will likely have a number of files (hard copy and electr...