Showing results for IRB

Broad Consent and Limited IRB Review
This module provides an in-depth look at the exempt research categories that require limited IRB review. Learners will explore the regulatory conditio...
A Recovering IRB Chair’s Guidance to Students Who Want to Do Research
Angela Bruch, PhD - Capella University Learning Objectives: Identify key guidelines for initial research phases. Understand the role of the...
IRB Chair Meeting Responsibilities
Describes critical areas related to preparation for the IRB meeting, the responsibilities associated with running an IRB meeting, and the activities a...
IRB Risk Assessment of Technologies in Human Subjects Research
The use of technologies, such as mobile apps, wearable devices, artificial or augmented intelligence (AI), machine learning, and nanotechnology, will ...
IRBs, Safety Review, and Monitoring
This module discusses the major milestones in the history of human subjects research that have affected current research regulations and practice. It ...
The IRB Administrator’s Responsibilities
Provides the foundation for the IRB administrators’/directors’ responsibilities including communication, interpretation and implementation of regu...
External Oversight of the HRPP/IRB: Monitoring and Inspections
Focuses on monitoring and inspections of HRPPs/IRBs. Monitoring and inspections are both types of external oversight provided by study sponsors and re...
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