Instant Focus on Critical Risks
Automatically surfaces what matters most, no more manual data sifting.
Confidence in Decision-Making
Clear, data-backed insights empower timely and informed actions.
Efficiency Gains of Up to 30%
Streamlined workflows and reduced monitoring overhead.
We’re excited to connect with you at PCMG 26! Whether you're just starting your RBQM journey or looking to optimise your approach, our team is here to guide you toward smarter, more efficient trials.
Let’s talk about how TRI can support your goals with confidence and clarity.
At TRI, we make Risk-Based Quality Management simple and effective, helping sponsors and CROs cut down on manual work, and achieve better clinical outcomes with confidence.
Our Good Clinical Practice (GCP) e-Learning just got even better. It’s now CPD Certified. So not only will you stay compliant, your training will count toward your professional development too.
We'd like to offer you a trial of our new GCP e-Learning module, including ICH E6(R3) updates.
What you’ll learn:
Simply hit the Register Now button below, and we'll set you up.
✅ CPD Certified
✅ Flexible, online learning
✅ Perfect for clinical research professionals
TRI are experts in Risk-Based Quality Management, with deep expertise and a proven platform designed to simplify compliance and accelerate clinical trial outcomes.
Our vision is to make critical data count, because every patient matters.
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TRI has delivered clinical trial tools since 2013. We launched our Centralized Monitoring service in 2016 and added our Risk Assessment and Management module in 2020.
We assign a full implementation team to each client. Support includes:
We also train your system admins and super users. Online training videos are available before and after launch. Soon, we’ll add a support hub within the OPRA app for easy access to help content.
Yes. The platform uses tailored data charts and statistical models for each clinical trial. These tools help spot patterns, trends and data issues. The systems design makes it easy to view and act on these insights.
OPRA supports all key RBQM processes for clinical trials, as defined in ICH E6 R3 and earlier guidelines. It enables sponsors and CROs to effectively manage quality and risk throughout the entire clinical trial lifecycle.
TRI works closely with leading groups like ACRO, PhUSE, and TransCelerate. We also learn from our user community and apply best practices in each platform update.
