Non-English Speaking Research Subjects: What’s in the Regs?
Recently, the clinical research community has been making efforts to include more diverse subject populations in clinical studies. Sec. 907
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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
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
The Six Characteristics of an NCI-Designated Cancer Center
Learn the key characteristics that all NCI-designated cancer centers have in common.
“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 an Electronic Data Capture (EDC) System
This post walks you through the basics of an electronic data capture system, providing a high-level overview of benefits and common functionality.
Deciphering the CRC Career Path: Key Skills and Responsibilities
Wendy Tate, Director of Data Analytics at Forte, explains key skills and experiences sites look for in a clinical research coordinator.
Beginner’s Guide to Clinical Trial Performance Metrics
Basics to help you get started measuring and improving your clinical trial performance.