Showing results for IRB

FERPA and Online Learning in the Time of COVID-19
This webinar explores how the Family Educational Rights and Privacy Act (FERPA) (20 U.S.C. § 1232g; 34 CFR 99) applies to online learning. The presen...
Summit: Welcome to Clinical Research
This course introduces the fundamental principles and practices of conducting clinical trials. It examines the functions of study protocols, the requi...
Institutional/Signatory Official: Human Subjects Research
Institutional/Signatory Official: Human Subjects Research provides a general introduction for institutional officials (IOs) in a variety of organizati...
ICH E6(R3): An Introduction
The course describes the ICH’s Guideline for Good Clinical Practice E6(R3). E6(R3) includes several updates from E6(R2). This video-based course exa...
Summit: Participant Recruitment
This course describes methods for building trust with participants who are a “good fit” for the clinical trial. The course explains the importance...
On Research Podcast - Improving Access to Research Studies
Season 2 - Episode 5 - Improving Access to Research Studies Access to research is a complicated but essential area of growing concern in the research...
Explore the FDA's New Guidance on Expanded Access Submissions
Introduction The U.S. Food and Drug Administration (FDA) is critical in ensuring patient access to investigational drugs and biological products thro...
FDA Draft Guidance on Protocol Deviations in Clinical Trials
The FDA recently issued draft guidance titled “FDA Guidance on Protocol Deviations,” which provides critical insights into managing protocol devia...
On Research Podcast - CITI Program Turns 25: A Celebration of Commitment to Research Integrity
Season 3 - Episode 4 - CITI Program Turns 25: A Celebration of Commitment to Research Integrity This episode is a celebration of CITI Program’s 25t...
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