More than a Signature.

Consent is one of the first and most important
patient touch points.

Sitero’s unique eConsent offering is adaptable and made for modern clinical trials. It is designed to meet the real-world needs of sponsors, CROs, sites, IRBs, and most importantly, clinical trial participants.

NATIVELY INTEGRATES WITH:

LATEST UPDATES

Enhanced Feature Set Launched April 2025!

Check back regularly for the latest improvements and platform news.

Sitero eConsent - Clinical Trial Sitero

Why Mentor eConsent?

  • INFORMED CONSENT: Empowering participants to make informed decisions.

  • WORLD HAS GONE DIGITAL: A digital world demands digital consent.

  • RISK MITIGATION: Ensures participant understanding and increases participant conformance.

  • QUALITY: Guarantees the participant always consents using the most current IRB approved version of the informed consent document.

Mentor eConsent Key Metrics

30+ CLIENTS | 100+ STUDIES | 1,000+ USERS | 50 COUNTRIES SERVED

SPEED

68%

DECREASE
in Time to Consent

COST

56%

DECREASE
in Administrative Costs at the Site/Sponsor

TIME

40%

DECREASE
in Consent Document Approval Time

QUALITY

20%

INCREASE
in Participant Retention

DATA

100%

GUARANTEE
Transparent Real-Time Reportability

Mentor eConsent Features

Built for global flexibility and regulatory confidence. Designed to integrate seamlessly with RTSM and EDC. Multimedia and multilingual options ensure participants make informed decisions.

Out of the Box Template Libraries

Fully Enabled for Remote Consent Used Globally

Supports Multiple Consenter Types

Multimedia and Multilingual (26) Consent Options

Out of the Box Integration with RTSM and EDC

Key Differentiators

Mentor eConsent combines robust tools with participant-centric design—streamlining compliance, customization, and oversight across studies.

eConsent Software - Screenshots - Sitero

  • Batch administration of consent documents.

  • Rapid site-specific form creation.

  • Version control for consent and reconsent.

  • Dashboarding for monitoring ease.

  • Knowledge checks.

  • Document categories (Consent, HIPPA, etc.).

  • Automated reconsent/consent expirations.

  • Withdraw consent workflow.

eConsent Accelerated Implementation

Get started quickly with a dedicated implementation team to enable and inform patients today.

eConsent Timeline - Clinical Trial Services Sitero

Testimonial

“Our team has been impressed with the eConsent platform—it’s intuitive, easy to implement, and has improved participant comprehension. The multimedia tools helped simplify complex study details, leading to faster enrollments and stronger engagement. It’s also streamlined our compliance process and boosted confidence in our consent records.”

Director of Clinical Operations

eConsent Resources

Learn more about digital consent trends and best practices. Explore our latest blog posts and check back soon for new insights.