The Only EDC Software Designed For Small and Scaling Clinical Teams

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EDC SOFTWARE

The Only EDC For Small and Scaling Clinical Teams

No-code, point-and-click configuration

Same clinical rigor as enterprise EDCs

Go live in days instead of weeks

See how easy Medrio is to set up and run with a demo

SurveyRight vs. DIY Tools

VALIDATED CONTENT

GENERIC FORMS

THIRD-PARTY CANDOR

INTERNAL BIAS CONCERNS

DRIVER-RANKED PRIORITIES

ISOLATED SCORES

BENCHMARKS & TREND VIEWS

STATIC RESULTS

MANAGED DELIVERY

HEAVY INTERNAL LIFT

Frequently Asked Questions

FAQ Accordion

01 How fast can we go live with Medrio EDC?

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Medrio is built for fast setup. It's incredibly easy to learn, and designed to allow teams to go live in only hours or days vs. weeks or months!

02 Can we make mid-study changes without downtime?

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Yes. You can test changes before they go live, then roll updates out without downtime. That means protocol changes and form updates do not have to disrupt sites or derail timelines.

03 How does Medrio support compliance and inspection readiness?

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Medrio includes the controls teams rely on for regulated trials, including validated electronic records and signatures, full audit trails, role based access controls, and encrypted data. It is designed to align with common requirements like 21 CFR Part 11, ICH E6(R2), HIPAA, and GDPR, while supporting long term access through secure backup, disaster recovery, and flexible exports.

04 Does Medrio integrate with eConsent, RTSM, eCOA/ePRO, and other systems?

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Yes. Medrio connects with eConsent, RTSM or IRT, eCOA and ePRO, safety systems, and other eClinical tools. It also supports standard data capture and export workflows to reduce manual reconciliation and keep systems working together cleanly.

“Medrio has all the features necessary to capture data for any clinical trial. They present it in a very easy to use interface that sites like to use. The design features allow for rapid setup and deployment which is key for many types of clinical studies.”

–Stephen B.
SVP Business Development and Commercial Strategy Pharmaceuticals

All the control, none of the coding.

POWERING TRIALS FOR EMERGING INNOVATORS

Life Sciences Teams Are Stuck With Two Options:

THE PROBLEM

Medrio Bridges the Gap for Growing Clinical Teams

THE SOLUTION

Build Your Study With Ease

NO-CODE STUDY BUILDS

Create eCRFs, logic, and workflows with point-and-click configuration, then save them to reuse as templates so you never have to build from scratch.

Make Mid-Study Updates Without Derailing Timelines

ZERO-DOWNTIME AMENDMENTS

Test changes before they go live, then roll them out without downtime. Updates feel routine and are deployed with confidence.

See What’s Happening as It Happens

REAL-TIME DATA VISIBILITY

Use dynamic dashboards and reports to spot issues early, answer questions fast, and keep the study moving.

Get Expert Tools You Can Trust

PROVEN CLINICAL RIGOR

Experience a fully validated, audit-ready EDC backed by 20+ years of clinical use across thousands of trials.

“I’ve been using Medrio EDC at my current company for about three years, and it’s genuinely one of the most user-friendly and reliable data-capture systems I’ve worked with. The platform is intuitive and easy to navigate, which makes it simple not only to build and configure studies but also to train site staff — even those with limited prior EDC experience.”

–Verified User in Biotechnology

9.6k+

83%

98%

65%

Studies deployed globally

Faster mid-study changes

Faster study builds

Of teams stay with Medrio

Made for the Reality of Small Teams Running Serious Trials

See Medrio in action with a free live demo.

Upholding the Highest Compliance Standards