Centralized Monitoring

Made Simple

Elevate your trial oversight. OPRA-CM enhances centralized monitoring for clinical trials with a smarter and more efficient RBQM approach, simplifying complexity to proactively identify risks and take faster action.

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About OPRA-CM

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Success Stories

ABOUT OPRA-CM

Centralized monitoring, reimagined

OPRA-CM transforms centralized monitoring by providing instant focus on critical risks, instilling confidence in decision-making, and driving efficiency improvements of up to 30%.

The easy-to-use platform empowers teams to streamline risk-based monitoring and take timely, data-backed actions with clarity and confidence.

Focus
Confidence
Efficiency

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Focus

Focus on critical risks

OPRA-CM goes beyond simply aggregating data - it directs attention to what truly matters. Instead of overwhelming users with endless charts and metrics, it highlights key areas of concern, guiding teams to the insights that require action. With a clear view of trends over time and the ability to drill down into specific risks, teams can quickly monitor clinical trial risk and take appropriate action.

Instantly visualise changes over time
Uncover hidden insights
Quickly identify areas of concern

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Confidence

Make assured decisions

Decision-making is at the heart of RBQM. OPRA-CM removes uncertainty with a dynamic view of risk indicators that track trends over time instead of relying on static snapshots. Its intelligent data structure overlays key metrics to provide context and help teams adapt to emerging risks. With complete visibility into study, site, and subject data, teams can make informed decisions with clarity and certainty.

Ensure complete data visibility
Adapt to emerging risks and changes
Facilitate evidence-based decision making

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Efficiency

Be more effective

With growing pressure to do more with less, OPRA-CM lets technology do the heavy lifting. Pre-defined workflows automatically create and update monitoring observations, reducing manual effort and keeping review logs up to date. Teams can seamlessly review, track, and manage monitoring alongside their data. By automating routine tasks and simplifying periodic reviews, OPRA-CM focuses resources on critical risks and activities.

Create rules and automate record creation
Streamline periodic review
Prioritize high value activities

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Reporting

H2

Feature

Unlock seamless risk communication with OPRA RAM's Advanced Reporting Capabilities. This feature is designed to streamline the way you share and communicate risk information, eradicating the complexities associated with traditional document sharing. With options for generating PDFs and bespoke reports, OPRA RAM ensures that you can tailor your risk communication to meet the specific needs of your stakeholders. These advanced reporting tools not only enhance clarity and understanding but also facilitate a more efficient exchange of critical risk-related data.

Feature

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Clinical trial risk management tools

Data Visualization Tools

OPRA-CM

Real-time insights

Availability of up-to-date risk scores

Trend analysis

View evolution of risks over time

Collaboration

Centralized portal to collaborate with stakeholders

Alerts

Customizable alerts

Data visualizations

Customizable data visualizations

Version control

Eradicates duplication

Assign actions

Assign actions to stakeholders

Document corrective actions

Document key information

Audit ready

Full discoverability of mitigations after closeout

FAQs

We've got the answer

Explore our FAQs for answers and expert advice on RBQM.

What is RBQM in clinical research?

Yes, you can try us for free for 30 days. If you want, we'll provide you with a free 30-minute onboarding call to get you up and running.

What is the difference between RBM and RBQM?

Of course you can! Our pricing scales with your company. Chat to our friendly team to find a solution that works for you as you grow.

What is the difference between RBM and RBQM?

Of course you can! Our pricing scales with your company. Chat to our friendly team to find a solution that works for you as you grow.

What is RBQM in clinical research?

Yes, you can try us for free for 30 days. If you want, we'll provide you with a free 30-minute onboarding call to get you up and running.

What is the difference between RBM and RBQM?

Of course you can! Our pricing scales with your company. Chat to our friendly team to find a solution that works for you as you grow.

What is the difference between RBM and RBQM?

Of course you can! Our pricing scales with your company. Chat to our friendly team to find a solution that works for you as you grow.

TESTIMONIALS

RBQM Success Stories

Hear directly from our partners about how we've helped them.

Peter Benton President & CEO, Worldwide

Worldwide’s RBQM team is one of the most experienced CRO teams in the industry. This, coupled with TRI’s best-in-class technology, ensures we can proactively identify and manage risks, meaning improved quality and patient safety, and, in turn, provide a better experience for sponsors and patients.

Jeff Smith Former CEO, Alimentiv

What truly set TriTrials apart from other vendors was their unparalleled commitment to a quality deliverable helping us effectively apply a novel approach to our operations. They achieved a deep understanding of our objectives by partnering with us on a rigorous change management process which culminated in a shared vision for the integration of their risk assessment and central monitoring solution.

Amandeep Sonik Senior Director, RBQM, Worldwide

The Worldwide Clinical Trials team is pleased with our continued partnership with TRI and we are excited about the milestone of having 150 clinical trials in TRI's Risk-Based Quality Management platform. This is a key benefit for our customers as it improves data quality, trial efficiency, and patient safety.

Kelly Parish Holladay AD, RBQM, Worldwide

It has been such a wonderful ride with our TRI partners over the last few years developing our RBQM strategy with our Sponsors and Worldwide Clinical Trials Teams! We love working with everyone at TRI and look forward to bigger and better things to come!