Medrio EDC

What is Medrio All About?

We’re scientists, analysts, writers, accountants, moms, dads, and weekend warriors. We’re Medrio. And the one common denominator we all share is that we’re confident our technology makes your trials run more efficiently. This drives everything we do. It’s why we return to our computers each morning, and it challenges us to build even better solutions that advance us toward a healthier world.

5,500+

Studies

1M+

Participants

36,000+

Sites

98%

Satisfaction Rate

Helping You Help Your Patients

We formed our company 15 years ago because clinical trial technology shouldn’t be challenging to use. That’s still our guiding principle today as we passionately and expertly develop intuitive and innovative solutions that put you in the driver’s seat (don’t worry, though–we include the manual).

Decentralized Clinical Trials (DCT)

We’ve been innovating eClinical software since 2005 with the intention of simplifying workflows for clinicians and patients. Our Decentralized Clinical Trials Solution is no different. We offer a unified ePRO/eCOA, eConsent, DDC, and RTSM with our EDC. And all of our solutions are designed to meet you where you are and help you reach your goals—in a traditional, hybrid, or fully virtual environment.

Begin Your Decentralized Journey Today

Direct Data Capture (DDC)

Source data validation (SDV) is necessary but time-consuming. Give your sites some valuable time back by empowering them to collect data directly from the source (on or offline) and reduce SDV headaches.

Say Hello to DDC and Goodbye to SDV Headaches

Electronic Consent (eConsent)

People find consent forms tedious to read and full of complex legal language. As a result, participants are less likely to grasp what is fully expected of them and more likely to drop out later. Our electronic consent tool lets you use plain language and even incorporate video or illustrations to increase understanding and reduce patient drop-out rates.

Help Me Improve My Consent Process

Electronic Data Capture (EDC)

Our user-friendly EDC interface makes it possible for you to build your entire study the way you want it. Its intuitive design means that you don’t need a programmer for every small or mid-study change. But if you find yourself in a jam or need any sort of help, our support team is ready 24/7 to assist you.

Help Me Achieve FPI Faster

Electronic Patient-Reported Outcomes (ePRO)

Our web-based ePRO solution makes it easier for your patients to report how they are feeling. And get this – it works on any device, anywhere. Whether your patients use it on their home iPad, or your staff access it on a clinical tablet, you can always count on timely and reliable data.

Learn More About Our Remote Data Collection

Randomization and Trial Supply Management (RTSM)

We know randomization can make or break a study. What if a single solution could help you reduce site overages by 20 – 40% while increasing patient compliance and meeting all of your randomization needs? It would be a game-changer, and we’re here to tell you – we’ve changed the game.

Learn More

Professional Services

We want you to succeed. Sometimes you need a little extra help to reach your goals. Lean on our experts for everything from study builds, licensing, translations, and more!

Better Together? Tell Me More

Traditional, Virtual, or Hybrid Trials - We’ve Got You Covered

Since 2005, we’ve been innovators in the eClinical space, evolving right alongside our customers to meet the demands of today’s world. The solution to your next trial might be a combination of the many tools we offer. If you’re unsure of which type of trial you need, our experienced team can walk you through how the decentralized trial process works.

Committed Customer Service

Trials conducted across the globe depend on our technology, which means our global support team is ready to help you any minute of any day. When you talk with them, you’ll immediately see that they love their job and wear their 98% customer satisfaction rating like a badge. Yes, our tools are intuitive and user friendly, but if you need help getting started, building, or even changing your study midstream, don’t hesitate to ask. You’ll be glad you did.

Be Confident Your Data is Secure and Compliant

We take the security and compliance of your data and your participant’s privacy very seriously.

Having supported trials around the world, our analysts get it. We worry about the complexity of global security regulations, so you don’t have to. We also work closely with external auditors to ensure we’ve followed all of the necessary software and procedural controls.