Evaluating eConsent: Some Considerations from an IRB Perspective
At Advarra we’ve been seeing more and more eConsent studies recently, which is great—eConsent technology can often better inform participants
Reviews
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
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. In studies
IRB Review of Adaptive Design Studies
The popularity of adaptive design in clinical research continues to grow. Adaptive design can be more efficient than traditional study
“Single IRB” vs “Central IRB” – What’s the Difference?
With the rise of single IRB (sIRB) mandates, understanding the nuances between sIRB and central IRB (cIRB) is crucial for multisite studies.
Beginner’s Guide to Clinical Trial Performance Metrics
Basics to help you get started measuring and improving your clinical trial performance.