09/02/2026
If you've ever considered participating in a clinical research study, you may have heard the term IRB.
Before a study can begin, the IRB carefully reviews the research plan to help ensure:
✔️ Participant safety is the top priority.
✔️ Risks are minimized whenever possible.
✔️ Participants receive clear, understandable information before deciding to join.
✔️ The study is conducted ethically and follows strict federal regulations.
The IRB continues to monitor research throughout the study, not just before it starts, helping ensure participants remain protected every step of the way.