Clinical Trial Technology

From research
to results,

we’re here to empower your clinical trials.

For 20 years, innovative clinical trial sponsors and CROs have trusted Medrio. Our technology is built to handle complexity without compromising ease of use, so you can focus on the results.

Studies deployed globally
0 K+
Faster database lock
0 %
Customer retention rate
0 %
Faster mid-study changes
0 %

TRUSTED BY DYNAMIC THOUGHT LEADERS

Your trusted partner for every step of your trial.

With two decades leading the industry, Medrio understands your unique challenges. Get personalized support while benefitting from our global reach, expert guidance, and robust resources.

Test drive your study

  • Expert protocol reviews
  • Hands-on trial sandboxes
  • Personalized demos

Launch your trial with ease

No-code, quick-start technology with 24/7 global support always included.

Run smarter,
faster trials

Proactive guidance to efficiently scale trials to commercialization.

Streamline
your trial,
end-to-end

  • Unified EDC platform
  • Participant solutions
  • Flexible RTSM program

Medrio gives you control
without complexity

Medrio’s unique approach of “guided autonomy” brings unmatched benefits compared to standalone self-service options and bloated legacy solutions.

Unexpected DIY workload

Unexpected DIY workload

Missing or paywalled support resources

Missing or paywalled support resources

Hidden fees and surprise costs

Hidden fees and surprise costs

Uncertain vendor stability

Uncertain vendor stability

Missing critical features

Missing critical features

Disconnected data silos

Disconnected data silos

Takes weeks—not months—to go live

Takes weeks—not months—to go live

Go live in as little as two weeks, versus the industry average of 68 days, with our intuitive, no-code platform.

Always-on, fast support

Always-on, fast support

Trust our 24/7 global support for rapid assistance, with initial responses in under 10 minutes and more than 75% of requests resolved within 24 hours.

Intuitive for all users

Intuitive for all users

Empower builders with a point-and-click interface to configure studies quickly. Offer sites an intuitive, streamlined workflow for faster, more accurate data entry to enhance productivity for the entire team.

Zero-downtime mid-study changes

Zero-downtime mid-study changes

Adapt to evolving study needs with ease. Medrio allows for mid-study changes in as little as a day, with zero downtime, ensuring your research remains on track.

Unwavering reliability & compliance

Unwavering reliability & compliance

Ensure your study remains compliant and audit-ready on our fully validated platform, engineered for unwavering stability. Comply effortlessly with global standards like ISO 9001, GDPR, and 21 CFR Part 11.

A single source of truth

A single source of truth

Experience truly connected data flow across your entire trial. Our single, integrated platform offers EDC, RTSM, ePRO, eConsent, and more. This approach reduces risks like duplicate entry and lag time, offering direct data access and insights at your fingertips.

Lengthy, resource-intensive setups

Lengthy, resource-intensive setups

Frustratingly slow support

Frustratingly slow support

Cumbersome midstudy changes

Cumbersome midstudy changes

Steep learning curve for new users

Steep learning curve for new users

Surprise fees and coding cost

Surprise fees and coding costs

Challenging exports and data access

Challenging exports and data access

Unexpected DIY workload

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Missing or paywalled support resources

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Hidden fees and surprise costs

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Missing critical features

Sed ut perspiciatis unde omnis iste natus error sit voluptatem accusantium doloremque laudantium, totam rem aperiam, eaque ipsa quae ab illo inventore veritatis et quasi architecto beatae vitae dicta sunt explicabo. Nemo enim ipsam

Disconnected data silos

Sed ut perspiciatis unde omnis iste natus error sit voluptatem accusantium doloremque laudantium, totam rem aperiam, eaque ipsa quae ab illo inventore veritatis et quasi architecto beatae vitae dicta sunt explicabo. Nemo enim ipsam

Go live in as little as two weeks, versus the industry average of 68 days, with our intuitive, no-code platform.

Trust our 24/7 global support for rapid assistance, with initial responses in under 10 minutes and more than 75% of requests resolved within 24 hours.

Empower builders with a point-and-click interface to configure studies quickly. Offer sites an intuitive, streamlined workflow for faster, more accurate data entry to enhance productivity for the entire team.

Adapt to evolving study needs with ease. Medrio allows for mid-study changes in as little as a day, with zero downtime, ensuring your research remains on track.

Ensure your study remains compliant and audit-ready on our fully validated platform, engineered for unwavering stability. Comply effortlessly with global standards like ISO 9001, GDPR, and 21 CFR Part 11.

Experience truly connected data flow across your entire trial. Our single, integrated platform offers EDC, RTSM, ePRO, eConsent, and more. This approach reduces risks like duplicate entry and lag time, offering direct data access and insights at your fingertips.

Lengthy, resource-intensive setups

Sed ut perspiciatis unde omnis iste natus error sit voluptatem accusantium doloremque laudantium, totam rem aperiam, eaque ipsa quae ab illo inventore veritatis et quasi architecto beatae vitae dicta sunt explicabo. Nemo enim ipsam

Frustratingly slow support

Sed ut perspiciatis unde omnis iste natus error sit voluptatem accusantium doloremque laudantium, totam rem aperiam, eaque ipsa quae ab illo inventore veritatis et quasi architecto beatae vitae dicta sunt explicabo. Nemo enim ipsam

Cumbersome midstudy changes

Sed ut perspiciatis unde omnis iste natus error sit voluptatem accusantium doloremque laudantium, totam rem aperiam, eaque ipsa quae ab illo inventore veritatis et quasi architecto beatae vitae dicta sunt explicabo. Nemo enim ipsam

Steep Learning curve for new users

Sed ut perspiciatis unde omnis iste natus error sit voluptatem accusantium doloremque laudantium, totam rem aperiam, eaque ipsa quae ab illo inventore veritatis et quasi architecto beatae vitae dicta sunt explicabo. Nemo enim ipsam

Surprise fees and coding cost

Sed ut perspiciatis unde omnis iste natus error sit voluptatem accusantium doloremque laudantium, totam rem aperiam, eaque ipsa quae ab illo inventore veritatis et quasi architecto beatae vitae dicta sunt explicabo. Nemo enim ipsam

Challenging exports and data access

Sed ut perspiciatis unde omnis iste natus error sit voluptatem accusantium doloremque laudantium, totam rem aperiam, eaque ipsa quae ab illo inventore veritatis et quasi architecto beatae vitae dicta sunt explicabo. Nemo enim ipsam

eBook

The State of AI in Clinical Trials

Asset Promo

Our relationship with Medrio helps us decrease timelines, especially with regard to study builds. Plus, real-time data management keeps our data clean and decreases database lock time.

Crystal Gates

Director of Clinical Operations, CTRG

CTGR_logo

Even though the Medrio system has a lot of features and can serve complex studies, we could still single out just the features we need—without sacrificing quality or service.

Lucia Cesnakova

Program Lead, Digital Medicine Society

DME

Medrio sets itself apart through its exemplary customer care and support, establishing a genuine working partnership. There is always someone available, assuring us that we are not alone.

Hannah Gillis

Head of Data Management, MAC Clinical Research

MAC_logo

With Medrio, we’ve got a much more effective workflow, allowing us to produce high-quality data without added headcount and focus on the research we are passionate about.

LaKeshia Scott

Associate Director of Data Management, Rose Research Center

RoseResearchCenter_Logo

I’ve spoken to other EDC companies that require their customers to have someone in-house who knows JavaScript or even deeper coding ability. With Medrio, all we need to know is how to write simple algorithms in Excel, which has saved a great deal of time and allowed us faster, easier access to our data.

Frances Rubenstein, PhD.

Director of Database Management, Nevro

NVRO_logo_white

Your integrated suite of solutions
on a unified platform.

Scalable, user-friendly solutions help streamline your trials. Experience real-time data access
and control to take trials further, faster.

eCOA/ePRO
CDMS-EDC
rtsm
Clinical-Data-Services
eConsent
Clinical-Trial-Project-Management
CDMS / EDC

Medrio CDMS / EDC

Leverage the full potential of your clinical data by combining data capture and management in one solution. More than just an EDC, Medrio’s clinical data management system (CDMS) combines an intuitive user interface and seamless data collection with comprehensive management tools.

EDC

Resources to help you get to market faster

Ready to see Medrio?

Book a live, personalized demo to see for yourself why clinical trial leaders trust Medrio.