Research Compliance
Evaluating eConsent: Some Considerations from an IRB Perspective
eConsent technology can often better inform participants than just the traditional paper consent, which is great from an IRB perspective.
Planning Gene Therapy Research? Plan for IBC Review
The completion of the human genome project and advances in genetic engineering have paved the way for clinical trials involving human gene transfer
Component Analysis: Analyzing Benefits and Risks of Individual Interventions to Ensure Appropriate Research Participant Protections
A major element of any IRB review is the examination of potential benefits and risks to study participants.
IRB Review of Adaptive Design Studies
Learn why the popularity of adaptive design in clinical research is continuing to grow!
“Single IRB” vs “Central IRB” – What’s the Difference?
Is there a difference between the terms sIRB and cIRB?
Beginner’s Guide to an Electronic Data Capture (EDC) System
An Electronic Data Capture system stores patient data collected in clinical trials. Learn the basics & functionality of EDC systems.
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