Resources

Found 21 Items.

Content Type	Title
Office	Institutional Review Board for Human Participant Research (IRB) Office
News	NIH Policy Change: New Data Management and Sharing Policy
News	Single IRB (sIRB) Regulatory Requirements in Effect January 20, 2020
News	Collaborative IRB Process for Cornell University and Weill Cornell Medicine
News	GDPR: European Data Regulation Impacts Research
News	Changes to Research with Human Participants: Revisions to the Common Rule
Process	Compliance, Ethics, Safety
Resource	IRB Announcements & Newsletters
Resource	IRB COVID-19 FAQs
Resource	Submit or Manage Your IRB Protocol
Resource	IRB Informed Consent
Resource	IRB Training
Resource	IRB Considerations: Human Participant Data, Data Sets and Internet Research
Resource	IRB Biomedical Research
Resource	IRB Considerations for International Research
Resource	IRB Considerations for Clinical Trials
Resource	Multi-site and Collaborative IRB Research
Resource	Report a Concern Involving Human Participant Research
Resource	About the IRB Committee
Resource	IRB FAQs
Resource	IRB Guidance and Resources