Make Informed Consent Easier To Complete And Manage

Schedule Demo

ELECTRONIC CONSENT SOLUTION

Remote, onsite, and paper workflows in one process

Automated tracking of consent and IRB status

Multi-signer and multi-site signature capture

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

POWERING TRIALS FOR EMERGING INNOVATORS

“Medrio is very easy to work with in terms of building clinical trial databases from beginning to end. I've also heard that the end users are happy to use this product. The customer service is amazing!”

–Sally M
Senior Clinical Data Manager Research

A Smoother Way To Handle Consent for Trials

See Medrio in action with a free live demo.

Upholding the Highest Compliance Standards

Support every site without forcing one way of working.

Medrio Simplifies Consent Everywhere

THE SOLUTION

Run remote and onsite consent in one process

HYBRID CONSENT WORKFLOWS

Support electronic and paper consent side by side, so each site can follow what is required without breaking consistency across the study.

Help participants actually understand what they sign

PARTICIPATION COMPREHENSION TOOLS

Add images, video, quizzes, and FAQs to explain key study details clearly and improve retention, not just collect signatures.

See consent status in real time

CONSENT STATUS DASHBOARDS

Use built-in consent and IRB approval statuses and dashboards so you are not chasing sites or guessing where each participant stands.

Handle Updates without starting over

VERSION CONTROL AND RE-CONSENT

Manage consent versions and trigger re-consent when protocols change, with clear tracking that keeps you inspection ready.

“...the easiest to use and best EDC tool we have used to date and enables compliance with CFR 21 Part 11 (Annex 11). Medrio EDC is powerful yet much simpler to use than other products of a similar nature and has incredible customer support.”

–Glenn H.
Clinical Trials Database Manager Research

Most Consent Processes End Up in One of Two Traps:

THE PROBLEM

Frequently Asked Questions

FAQ Accordion

01 Can we do remote + onsite + paper?

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Yes. Medrio eConsent supports remote, in-clinic, and hybrid workflows, and it can also support paper-based consent when a site requires it. You can capture eSignatures where allowed, and upload wet-ink signed paper forms into the same workflow so everything is tracked and stored consistently.

02 Does it support versioning and re-consent?

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Medrio eConsent supports consent version control and re-consent. When a protocol change requires updated authorization, you can deploy the new version and track who has consented to which version, helping maintain traceability across the study.

03 How does it support compliance (Part 11, ALCOA++)?

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Medrio eConsent is 21 CFR Part 11 compliant, EU-compatible, and designed to meet ALCOA++ expectations through features like time-stamped electronic signatures, audit trails, role-based access controls, secure storage, and clear traceability of consent actions for inspection readiness.

04 How does it integrate with EDC/CDMS?

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Medrio eConsent is part of Medrio's unified clinical data platform, so consent status can be linked directly to study data in Medrio CDMS/EDC. That means sites and study teams can see consent status in real time and use it to support workflow logic and eligibility checks, reducing manual reconciliation.

05 What does implementation look like?

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Implementation is designed to be straightforward. Teams typically: 1. Upload and configure consent documents and workflows (remote, onsite, hybrid, and any paper handling) 2. Set up roles, signature routing, and versioning rules 3. Enable dashboards and statuses for consent and IRB oversight 4. Roll out with onboarding and enablement support from Medrio so sites know exactly how to use it