Bridging the Gap Between Human Research Participants, Investigators & Research Sponsors.
Opus IRB is focused on safeguarding the rights and
welfare of human research participants.
Our knowledgeable 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.