Learn about Cornell University's requirements for human participant research ethics (IRB) training, ...
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Informed consent is more than just a form; it is a process that takes place between researcher and p...
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...
An NDA is used to demonstrate an agreement to restrict disclosure of specific information exchanged ...
Center for Technology Licensing (CTL)
Center for Technology Licensing (CTL)
Commercializing Cornell Inventions The Center for Technology Licensing (CTL) is Cornell University'...
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...