ABOUT UNIVO
Unifying Patients and Research for the Benefit of All
Every protocol represents a person. That’s why Univo IRB’s mission is to unify patients and research through ethical review that ensures participants have a voice and clinical trials move forward confidently.
Univo IRB provides independent institutional review board (IRB) and research ethics board (REB) services throughout the United States and Canada, including:
- IRB and REB initial review and continuing oversight
- Central and single site review models
- Institutional biosafety committee (IBC) review
- Regulatory guidance and consulting
- Research compliance training
We support sponsors, CROs, and research sites with efficient, transparent review aligned with U.S. regulations, ICH GCP E6 R3, and Canadian standards, including TCPS2 and applicable provincial requirements. Through our OneVerse® platform, we offer responsive communication, practical guidance, and greater visibility, delivering an agile, reliable IRB experience that reduces uncertainty and simplifies the path to approval.
Backed by our dedicated customer service, proven regulatory experience, and unwavering commitment to patient advocacy, we do more than review research. We support it, strengthen it, and help bring new therapies to patients with speed, clarity, and confidence.
FEATURED ARTICLES
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![predictive medical analytics, digital AI interface, patient data, DNA insights-GettyImages-2262212753]( "It's A Mad Men World For IRB Review Of Clinical Trial Advertisements")
Modern digital tools and AI have transformed clinical trial recruitment, outpacing decades-old regulations. Discover how to apply core ethical principles to protect participant privacy and equity.
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![Medical team, tablet, meeting-GettyImages-2177971058]( "Real-World Evidence Revisited")
Explore how the latest regulatory updates transform real-world data into a credible evidentiary pathway. Learn the new standards for data reliability and hybrid study design.
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![GettyImages-2200850893-US-FDA-Food-Drug-Administration]( "General Wellness Isn't A Vibe Anymore: What The 2026 FDA Update Means")
The FDA’s 2026 guidance has put an end to "wellness by disclaimer." Learn how new standards for wearables and apps impact study design, participant safety, and the evolving ethical role of the IRB.
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![coding, application development, software-GettyImages-2012746930]( "Clinical Decision Support Software: Clear Expectations For Research Oversight")
The FDA’s 2026 CDS guidance signals a shift to settled policy. IRBs must now demand greater transparency regarding automation bias and clinician independence to accurately assess study risk.
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![GettyImages-1551861554-FDA]( "The FDA's Final BIMO \"Processes And Practices\" Guidance")
Gain a clear roadmap for investigators, sponsors, and IRBs. This shift toward transparency replaces regulatory guesswork with predictable standards for every partner in the research ecosystem.
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![GettyImages-1245953899 IRB compliance]( "What Does The FDA's 2025 Safety Reporting Guidance Mean For You?")
New FDA guidance aligns IND safety reports with unanticipated problems, shifting the focus from administrative definitions to proactive participant protection and trial integrity.
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![business contract signing-GettyImages-1223604108]( "Clinical Research Update: The New FDA Form 1572 is Available")
The FDA released an updated Form 1572, approved through September 30, 2026. Stay current with the new form to ensure seamless compliance for your next clinical trial update.
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![Global health safety regulation-GettyImages-2245658628]( "FDA Updates Guidance For Written IRB Policies")
Explore how updated FDA and HHS guidance harmonizes regulations, streamlines IRB operations, and strengthens oversight for complex clinical trials.
FEATURED VIDEOS
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![Female researcher analyzing scientific samples-GettyImages-2231025177]( "Unifying Research - Tribal Health And Research And Patient Michele")
Kelsey Powell explores the urgent need for better clinical research access in tribal healthcare, while Michele Baptista shares how her cancer journey led to a research opportunity that changed her life.
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![GettyImages-1938542776 doctor patient]( "Unifying Research - HRPP Vs IRB And Participant Christine")
HRPPs and IRBs play different but connected roles in protecting research participants. Hear expert guidance, firsthand experiences, and questions that can help people make more informed decisions.
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![HCP speaking with a patient in an exam room (high res) (1)]( "Unifying Research - Research Administration And Participant Caregiver")
Go behind the scenes of cancer clinical trials operations and hear a caregiver’s perspective on supporting a research participant, including the challenges, needs, and opportunities.
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![Meeting, team, medical case review, treatment plan, research-GettyImages-2265129844]( "Unifying Research - Research Compliance And Patient Stephanie")
A research compliance leader and a patient advocate explore how ethical oversight, privacy, and the IRB intersect while sharing a personal PMDD journey that shows the potential of participation.
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![AI, artificial intelligence-GettyImages-2224574999]( "Unifying Research - Patient Negative One And Christine Von Raesfeld")
Clinical research innovation and patient advocacy meet in a conversation about AI, ethics, autonomy, and trust, highlighting how bold ideas and lived experience help shape a more responsible future.
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![Welcome to the future]( "A More Intuitive IRB Submission Experience")
Gain insight into a more intuitive IRB submission experience that can help reduce friction, improve transparency, and support today’s virtual research workflows.
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![Your IRB, Simplified: Fast, Friendly, And Focused With Univo IRB]( "Your IRB, Simplified: Fast, Friendly, And Focused")
IRB approval does not have to be defined by delays or confusion. Learn how expert guidance, regulatory support, and modern technology can help research teams move forward with greater efficiency.
CONTACT INFORMATION
Univo IRB
4509 Creedmoor Road, Suite 403
Raleigh, NC 27612
UNITED STATES
FEATURED SOLUTIONS
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![GettyImages-1220710526 lab, research]( "Clinical Research Consulting Services, Simplified")
Expert Support for Clinical Research and Research Administration
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![Univo Simplify]( "Independent IRB Approval, Simplified")
Partner with Univo IRB for the participant-centered service and forward-thinking technology you need to navigate a changing industry and get independent IRB approval, faster.
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![GettyImages-1759287088 patient nurse consultation]( "Eliminate Review Friction With An Industry-First IRB Platform")
Strengthen trial compliance and data integrity by mastering GCP through practical, real-world scenarios designed to prevent costly errors and ensure audit readiness across your research team.
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![GettyImages-1282633951-laptop-man-suit-office-quality-management]( "A Fast, Friendly, Fair IRB Designed For Modern Research Sites")
Strengthen trial compliance and data integrity by mastering GCP through practical, real-world scenarios designed to prevent costly errors and ensure audit readiness across your research team.
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![GettyImages-2161842577-business-professional-laptop-office-table]( "Overcome Biosafety Challenges With An Innovative IBC")
Simplify biosafety oversight and accelerate study startup with expert guidance that ensures NIH compliance while protecting researchers, communities, and the environment.
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![Training GettyImages-1366428092]( "Good Clinical Practice Training That Goes Beyond The Basics")
Strengthen trial compliance and data integrity by mastering GCP through practical, real-world scenarios designed to prevent costly errors and ensure audit readiness across your research team.
