CLINICAL TRIAL TECHNOLOGY

The Only EDC Built for Small and Scaling Clinical Teams

98% customer retention rate

20+ years of clinical trial experience

Thousands of completed studies

Medrio combines enterprise-grade rigor with no-code agility to help sponsors and CROs achieve more when every resource counts.

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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 What does Medrio’s platform include?
Medrio offers a unified clinical data platform including EDC, ePRO, eConsent, CTMS, and eTMF.
02 How quickly can Medrio EDC be implemented?
Studies can be configured and launched days to weeks using flexible no-code tools and reusable templates.
03 Who is Medrio built for?
Sponsors and CROs with scaling clinical teams that need enterprise-grade rigor without compromising speed, flexibility, and scalability.
04 How does Medrio improve data quality?
Built-in validations, real-time data access, and seamless workflows ensure clean, compliant, audit-ready data.

“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

Medrio supports research from early phase through post-market with a unified platform that brings your data, workflows, and teams together.

TRUSTED BY INDUSTRY LEADERS

Most EDC platforms force a compromise.

A platform that supports every study and phase

THE SOLUTION

Get power and flexibility with the EDC built just for you

Medrio delivers a fully validated, audit-ready EDC backed by 20+ years of clinical use and thousands of completed trials. Get expert support and high-quality data without the complexity, cost, or risk.

A platform that grows with every study and phase

Medrio supports research from early phase to post-market and everything in between. Scale easily with integrated EDC/CDMS, ePRO/eCOA, eConsent, and RTSM in an all-in-one platform.

Flexible no-code control for resourceful teams

Configure, adapt, and manage studies quickly without developers. Medrio gives sponsors and CROs full control to move faster without added complexity.

    83%     Faster mid-study changes

   60K   Faster database lock

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Ready to see Medrio?

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

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Bridge resource gaps with dedicated clinical experts who know your study inside and out.

Clinical Trial Project Management

Clinical Trial Data Services

Medrio offers support from seasoned project managers, data scientists, and product experts. From timeline acceleration to risk mitigation, we help you run smoother, smarter trials.

A team of 17 experts with 300 years of combined industry experience. Our expert service team can support you from database build and data management to biostatical analysis and regulatory-ready outputs.

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Connect to all your solutions

Medrio connects to the tools you already use through robust import and export APIs.

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Get expert support when you need it

Medrio integrates with the tools you already use through robust APIs and flexible data connections.

THE PROBLEM

Enterprise systems:

  • Too complex
  • Too rigid
  • Resource intensive

Lightweight tools:

  • Limited functionality
  • Disconnected data
  • No path to scale

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Automatically ingest data from wearables, sensors, and external devices.

Devices and eSource

Labs and LIMS

Import structured lab results, metabolic panels, and sample data from central, local, or point-of-care labs.

Export clean, machine-readable clinical and metadata to power
dashboards, reporting and advanced analytics.

Analytics and BI tools

Data lakes and warehouses

Stream complete clinical and study metadata into your data lake or warehouse for long term analysis and cross-study insights.