CCeConsent

Reduce Audit Findings and Increase the Quality of Your Consenting Process

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CCeSource

CCeConsent is the only electronic consenting system for sites that keeps patients engaged, ensures participant understanding, simplifies oversight and improves the overall consenting process.

Eliminate site ICP audit risks and boost patient retention with simple, interactive multimedia (text, video, audio, hints, multi-language) to keep patients engaged, while the system tracks progress and conducts knowledge assessments to verify participant comprehension throughout the consenting process. By simplifying the consenting process for staff with detailed analytics, remote access and real-time alerts and checks, sites also gain significant improvements in consenting efficiency and a boost in ICF data quality.

CCeConsent

Why CCeConsent ?

User Engagement

Boost Participant Engagement

  • Provides efficient digital capture
  • Minimizes double-data entry
  • Enables mobile device access

Enhanced Site Selection

Improve Patient Study Comprehension & Retention

  • Automated knowledge assessments
  • Hints for missed questions
  • Progress tracking and analytics

Compliance

Enhance Consenting Compliance

  • Standardized consenting eSignature process
  • HIPAA and CFR Part 11 compliance
  • Patients opt-out at any time

Tablet

Ensure Consent Process Efficiency

  • Standard regulatory and personal data forms
  • Consent versioning and audit trails
  • Automated reconsenting reminders

Improved Patient Engagement

Increase Patient Enrollment

  • Comprehension focused consenting
  • Easy to setup form templates
  • Complete process oversight

Quick

Start Visit Procedures Faster

  • Quality checks during consenting
  • Increased patient comprehension
  • Controlled eSignature workflow

Clinical Research Resources

CCeSource
Blog Post
The COVID-19 pandemic has caused an enormous disruption in healthcare priorities and staffing, and as restrictions on people’s movement have increased, clinical research sites face unprecedented challenges to adjust studies and patient engagement accordingly. The FDA has provided guidance to support ongoing continuity and response efforts, wherein the safety of trial participants is paramount. It […]

Increase Retention & Optimize Your Consenting Process

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