We recently welcomed Jan Hewett as our senior vice president, FDA regulatory advisor. With a decade of experience as regulatory counsel in the FDA’s Center for Drug Evaluation and Research – Office of Scientific Investigations, her experience will help Advarra’s clients and internal teams navigate the ever-shifting regulatory landscape for human subjects research.| Advarra - Advancing Better Research
What's new in Ruby 3.2's IRB? IRB 1.6 has been released and will become Ruby 3.2's built-in IRB version. It and a few recent releases include many enhancements @k0kubun and I made, and I want to introduce them in this article: New Commands In recent ...| Mostly Ruby DX
Improving IRB history. Some ways to improve your interaction with IRB history| Luca Pette
In the realm of academic research, the Institutional Review Board (IRB) process serves as a pivotal mechanism that ensures the ethical treatment of human| Robert Forto
Explore key local considerations for developing single IRB policies, and learn how to navigate the challenges- including compliance, ethical standards, and institutional requirements.| Advarra