Bridging the Gap Between Human Research Participants, Investigators & Research Sponsors.
Opus IRB is focused on safeguarding the rights and
welfare of human research participants. Highly experienced in all
aspects of clinical research, Opus IRB is one of the few commercial
Institutional Review Boards with
only actively practicing physicians from all across the country.
Our staff is comprised of individuals from all areas of research including the
pharmaceutical and medical device industries, private and public hospitals/universities,
clinical research clinics/sites
and clinical research auditing and compliance. Such diverse staff experience
from all aspects of the clinical research process and our comprehensive approach to monitoring
human research subject safety protects everyone involved.