Showing results for IRB

Understanding the New IRB Written Procedures Guidance from OHRP & FDA
Introduction The Office for Human Research Protections (OHRP) and the U.S. Food and Drug Administration (FDA) have released the final version of thei...
What is Research and What it isn't? And Who is a Human Subject Anyway? – Explaining the Common Rule in Plain Language
This webinar explains when an activity is or is not considered research, and who is or is not a human subject according to the Common Rule. The webina...
Before Saying “I Do” to the Common Rule: Figuring out “Engagement”
“Engagement” under the Common Rule often presents challenges to institutions and IRB administrators. This webinar takes a deep dive into the conce...
Institutional Review Board (IRB) Administration
Individuals responsible for the operations of IRB administrative offices and Human Research Protection Programs (HRPPs) play an integral role in the p...
Ethical Challenges and Considerations for IRB Review of Social Media Research
Overview Institutional Review Boards (IRBs) must consider various nuances when it comes to the review and approval of social media research proposals...
HHS Issues Draft Guidance on Limited IRB Review and Related Exemptions
Introduction The U.S. Department of Health and Human Services (HHS) recently released draft guidance on limited IRB review-related exemptions. Review...
Leading and Managing an IRB
This module describes best practices for effectively leading and managing IRB staff and an IRB board. From hiring practices and conflict resolution to...
Navigating Reliance Agreements and sIRB Review
In this module, learners will gain an understanding of the relationship between the relying institution and the reviewing IRB, including the reliance ...
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