eConsent for Clinical Trials

Faster enrolment. Full compliance.
Built into your trial from day one.

Replior eConsent replaces paper-based consent with a digital process that is faster to complete, easier for participants to understand, and fully audit-ready. Participants consent on any device, in their own language, on their own schedule.

Digital Consent for a Clinical Trial

Consent done properly, from the start

Informed consent is a regulatory requirement and a participant right. When the process is slow, confusing, or paper-dependent, it becomes a bottleneck before the trial has even started.

Replior eConsent makes consent fast, transparent, and compliant. Participants step through a clear digital process, confirm their understanding, and sign electronically. Updates and revocations are tracked automatically. Your team has a complete audit trail at every stage.

Replior eConsent

Manage the consent process to increase compliance and improve trial efficiency, integrated directly with your data collection strategy.

Maximize Participant Engagement

Participants who understand what they are agreeing to are more likely to complete the process and stay in the study. Replior eConsent is built to be clear, accessible, and respectful of their time.

Step-by-Step Guidance

Participants move through a structured consent process at their own pace, with each step explained clearly before they proceed.

Multi-Language

Offer consent forms in multiple languages, accessible on any device, to connect with a diverse audience.

Consent Revocation

Participants can withdraw consent at any time. The system records the revocation, updates all related records, and keeps your audit trail complete.

Streamline Trial Operations with eConsent

Streamline Trial Operations

Keep your trial running smoothly by integrating consent management right into your data collection process, saving time and reducing errors.

Seamless Integration

Consent data syncs with Replior EDC and eCOA/ePRO , as well as third-party systems, keeping all your trial data connected.

Automated Workflows

Cut down on admin work with automated tracking, updates, and data entry.

Efficient Data Handling

Simplify data collection and minimize errors with integrated workflows that keep everything in sync.

Unlock Valuable Insights

Gain clear, actionable insights into consent status and trial metrics with detailed reports that keep you updated at every stage.

Centralized Reporting

Get a clear overview of consent statuses and trial metrics with detailed reports in one centralized dashboard.

Customizable Exports

Generate reports in the formats that suit your team’s needs.

Real-Time Data Access

Track consent status in real-time with up-to-date data that helps you stay on top of key milestones.

Team of medical experts discuss innovative clinical trial - Replior

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FAQ

Replior eConsent connects with Replior EDC and eCOA (ePRO), as well as third-party systems, so all your consent data stays in sync and easily accessible.
Yes. Participants can revoke consent at any time. The system automatically tracks the change and updates all related data to keep everything compliant.
Replior eConsent supports compliance through version control, detailed audit trails, and real-time notifications, designed to meet a range of regulatory requirements.
Yes, we support multiple languages, making it easy to provide consent forms that are accessible to a diverse participant base.
Replior eConsent makes the consent process clear and accessible, with step-by-step guidance, mobile access, and multi-language support, so participants can understand and complete the process without friction.
Replior eConsent provides centralised reporting with customisable exports and real-time data access, so you can track consent status and trial metrics at every stage.
Yes. Replior eConsent uses encryption and secure access controls to protect participant data and ensure compliance with data privacy regulations.

Ready to simplify your consent process?

Ready to simplify your consent process?