Musculoskeletal
Is informed consent needed for post-market patient registry?
Blog Posts
The Role of IRBs in Research Oversight: Information for Research Teams to Support Diverse Research Participation
Whitepapers
The Role of IRBs in Research Oversight: Information for Potential Participants in Clinical Research
Whitepapers
Does the IRB need to approve doctor-to-doctor letters?
Blog Posts
What are the IRB review requirements for human factors/usability testing?
Blog Posts
Changes in Research: What are They and When do They Need to be Submitted to the IRB?
Whitepapers
Do You Know Me?: The Subtle Distinction Between “Anonymous” and “De-identified” Data in Clinical Research
Whitepapers
Can a physician submit a single humanitarian use device (HUD) submission to the IRB?
Blog Posts
Compensating Research Participants FAQ
Blog Posts