Bridging the Gap Between Human Research Participants, Investigators & Research Sponsors.

Opus IRB is focused on safeguarding the rights and welfare of human research participants.

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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.


Opus IRB Adds Senior Management Talent
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Notices, News and Events

Researcher Guide
Posted:  4/13/2012 9:03:31 PM

Overview for researchers including submission requirements, reporting responsiblilities resources...     More...


Compliance Issues
Posted:  4/19/2012 3:50:24 PM

To ensure the protection of human subjects, research compliance must be a priority.     More...