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Solutions

Electronic Consent Management System.

KEY TAKEAWAY

eTrialTrack eConsent supports digital consent workflows through structured content, version control, electronic signatures, consent status management and re-consent processes. The objective is to create a more organized consent workflow for participants, investigators and authorized study teams.

eCONSENT • PATIENT FIRST

What you get

Digital Consent Content
Multimedia Support
Version Control
Electronic Signatures
Consent Status
Re-Consent Workflows
Remote Consent Access
Connected Study Data
CONSENT ERRORS REDUCED
89%
Average across active customer deployments

What Is eTrialTrack eConsent?

eTrialTrack eConsent supports digital consent workflows through structured content, version control, electronic signatures, consent status management and re-consent processes. The objective is to create a more organized consent workflow for participants, investigators and authorized study teams.

Why Choose eTrialTrack eConsent?

Participant-Centered Workflow. eTrialTrack focuses on participant-centered workflow as part of a practical study workflow.

Controlled Documentation. eTrialTrack focuses on controlled documentation as part of a practical study workflow.

Operational Visibility. eTrialTrack focuses on operational visibility as part of a practical study workflow.

Connected Participant Journey. eTrialTrack focuses on connected participant journey as part of a practical study workflow.

Process-Based Compliance Approach. eTrialTrack focuses on process-based compliance approach as part of a practical study workflow.

How It Fits the Broader Study Workflow

Where appropriate, eConsent can be connected with other eTrialTrack capabilities to support a more coherent participant, site and data workflow. The exact configuration should follow the study protocol, organizational procedures, supported integrations and agreed implementation scope.

AUDIENCE & USE CASES

Who eTrialTrack eConsent is for

The eConsent module serves specific roles in a study team — here's who uses it, the use cases it supports, and when your study needs it.

WHO IT'S FOR
  • Site staff and principal investigators running consent discussions
  • Regulatory affairs teams tracking consent versions and approvals
  • Participants who need clear, multilingual consent on any device
USE CASES IT SUPPORTS
  • Remote and on-site electronic informed consent with e-signatures
  • Re-consent workflows when protocols amend mid-study
  • Version-controlled, audit-ready consent documentation
WHEN YOU NEED IT
  • When ethics committees require strict consent version control
  • When participants consent remotely in decentralized or hybrid trials
  • When paper consent creates storage, retrieval and compliance risk