Bridging the Gap Between Human Research Participants, Investigators & Research Sponsors.
Opus IRB Services
Opus IRB understands that in order to provide the best quality of human research subject
protection, all areas of the clinical research process should be understood. Our staff is
comprised of individuals from all areas of research including the Pharmaceutical/Medical
Device Industry, Private and Public Hospitals/Universities, Clinical Research Clinics/Sites
and from Clinical Research Auditing/Compliance.
Through diverse staffing from all areas of the clinical research arena, a well-rounded
approach to monitoring human research subject protection is achieved.
Our services include:
- An IRB panel comprised of specialties from across the country to provide a national
perspective for human research protection rather than regional
- IRB board meetings weekly to help facilitate timely submission turnarounds
- Experienced, knowledgeable staff who guide you through all the areas of the IRB process
from initial contact through the completion of a research study
- The OpusView® featuring a suite of online tools for managing studies under review
by Opus IRB including secure online forms submission for institutions/ sponsors and
provides applications designed to make the review process easier and more convenient
benefiting both Sponsors and Sites through greater efficiency, accuracy and more timely
responses to events throughout a study’s lifecycle
- Free online training program for Principle Investigators and Sub-Investigators regarding
oversight of clinical trials
Opus IRB Fee Schedule
An Opus IRB Fee Schedule is available upon request. Please contact us at
info@opusirb.com or complete the Contact Us form and click Submit.
You may also call toll free 1-877-346-8420