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.
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
- Unexpected DIY workload
- Missing or paywalled support resources
- Hidden fees and surprise costs
- Uncertain vendor stability
- Missing critical features
- Disconnected data silos
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
- Lengthy, resource-intensive setups
- Frustratingly slow support
- Cumbersome midstudy changes
- Steep learning curve for new users
- Surprise fees and coding cost
- Challenging exports and data access
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.
Director of Clinical Operations, CTRG
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.
Program Lead, Digital Medicine Society
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.
Head of Data Management, MAC Clinical Research
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.
Associate Director of Data Management, Rose Research Center
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.
Director of Database Management, Nevro
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.
Director of Clinical Operations, CTRG
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.
Program Lead, Digital Medicine Society
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.
Head of Data Management, MAC Clinical Research
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.
Associate Director of Data Management, Rose Research Center
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.
Director of Database Management, Nevro
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.
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.
Medrio eCOA/ePRO
Empower participants, clinicians, and observers to conveniently and accurately report outcomes, enhancing data quality and study efficiency. Medrio’s electronic clinical outcome assessment (eCOA) and electronic patient-reported outcome (ePRO) solution offers a user-friendly interface and flexible data capture options.
Medrio eConsent
Ensure compliance, increase comprehension, and empower efficient study management with Medrio’s electronic consent (eConsent) solution. Robust features, like multi-signer support and paper consent uploads, enable participants to consent from anywhere—remotely or onsite.
Medrio RTSM
Effectively randomize, manage, and control your trial supplies and minimize risks with our robust randomization and trial supply management (RTSM) solution. Advanced features enable you to configure allocation rules, automate shipment approvals, and receive issue notifications to streamline your supply chain process.
Clinical Trial Data Services
Accelerate study timelines, improve clinical data integrity, and enable internal teams with Medrio’s Clinical Trial Data Services. Our flexible services provide the support you need for effective, compliant clinical data management.
Clinical Trial Project Management
Empower your team and overcome resource constraints with seasoned project managers, data scientists, and knowledgeable product experts. From shortening study timelines to launching risk mitigation strategies, we help you expedite your clinical trials with ease.
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.