How the Best Research Teams Handle Informed Consent

FDAValidated
HIPAACompliant
IRBIntegrations
SOC IIPending

Accelerate Your
Clinical Trials

Generate compliant forms in minutes, not weeks
Get IRB approval 3x faster with ready-to-submit packages
Boost patient enrollment with 94% completion rates
ICF GENERATION

AI Generated ICF

Upload your protocol and get compliant consent forms in minutes. No more weeks of back-and-forth with legal teams.

Informed Patients =
Enrollment + Retention

Trustiva's interactive platform ensures patients truly understand their participation, leading to better retention and more successful clinical trials.

Multimedia

Multimedia

Interactive videos and visual explanations

Knowledge Checks

Knowledge Checks

Comprehension verification throughout the process

Q/A Directly with Sponsor

Q/A Directly with Sponsor

Real-time communication and support

Command Center

Version Control & History

Complete audit trails and rollback capabilities.

Amendment Management

Deploy amendments and track re-consent status.

Patient Status Monitoring

Real-time consent status and engagement metrics.

Trustiva Patient Dashboard showing consent management interface

Patient Consent Dashboard

Study Protocol: ONCO-2024-001

94%
Completed
156
Active
12
Pending
Patient 001-024Completed
Patient 001-025In Progress
Patient 001-026Amendment Required

Pricing That Scales
With Your Trial

From 10 patients to 10,000 - pay only for what you use. No setup fees, no surprises.

$25/patient

Complete consent process included

See Trustiva in Action

Experience how our platform transforms complex consent forms into intuitive, engaging digital experiences.

Trustiva platform interface showing consent form builder

Frequently asked
questions

Trustiva is built with regulatory compliance at its core. Our platform follows FDA 21 CFR Part 11 guidelines, maintains complete audit trails, and provides IRB-ready documentation. We work with regulatory experts to ensure all consent processes meet current standards and can adapt to evolving requirements.

Faster, compliant, informed
consent for clinical trials.