TrialConsent is an eConsent system that has been designed to meet both the user needs and regulatory requirements for the informed consent process.
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TrialConsent Self-Service and its Enablement
TrialConsent® Self-Service allows you to develop your own consent forms and documentation, create libraries for easy re-use across studies and maintain full control over your processes.
The University of Bristol Selects Signant Health's TrialConsent Solution in Oncology Trial
The Prestigious UK Academic Institution selected TrialConsent® to Administer eConsent to Benefit Sites and Patients in Future Clinical Research.
Signant Selected as eConsent Provider by Shanghai Mental Health Center
Signant Health has been selected to provide eConsent for a significant neuroscience study by the prestigious Shanghai Mental Health Center (SMHC).
TrialConsent Product Overview 2019
Introducing an eConsent solution that makes digitizing the consent process easy at any scale. Use TrialConsent® on your next small study, complex study, or even virtual study.
The Essential Guide to Electronic Informed Consent
14 Drivers of eConsent Adoption
Signant Health Partner Program
Become a CRO partner today. Sponsors what to know what your competitive edge is, so let's show them. We'll make sure you are distinguished and trusted for delivering across the Signant portfolio.
Enabling Electronic Informed Consent for Clinical Research Sites
Watch this information session on electronic informed consent designed exclusively for clinical research sites to see first-hand how eConsent can improve your informed consent process.
eConsent in Action - How It Works and Why Patients Appreciate It
In this 45-minute webinar on demand we discuss benefits for patients, sites and study teams, address common questions, and present a brief demo to help you make eConsent decisions for your trials.
Optimizing eConsent for Patient Centricity
Experts from across the clinical trial industry share their data, real case studies and expertise on how to best support patient centricity through eConsent.
CRF Health Looks To Simplify eConsent For Both The Patient And The Researcher
Clinical Informatics News and Rauha Tulkki-Wilke discuss eConsent adoption & how TrialConsent bypasses the eConsent setup hurdle for sponsors while delivering a patient-centered, easy-to-use solution.
The Top 10 Myths of Electronic Informed Consent
The top 10 myths about electronic informed consent (eConsent) and the journey that makes "going electronic" the only path for industry leaders.
Preparing for eConsent - A Step by Step Guide for Site Personnel
5 steps to help sites prepare for implementing an electronic informed consent (eConsent) solution.
Recruitment & Retention: Breaking Down the Barriers to eConsent Adoption
In Pursuit of eConsent: Best Practice Recommendations for Successful Integration
Provided by The Journal for Clinical Studies - Original at https://issuu.com/mark123/docs/jcs_volume_9_2_web/58 For more information about electronic informed consent please visit www.crfhealth.com
eConsent: Five (5) Key Areas of Preparation
Using eConsent in Clinical Research to Support Patient Understanding and Welfare
Deciding to participate in a clinical trial is not risk-free for anyone. This article explores how to best support patients during the informed consent process (ICP) with eConsent.
CRF Health Scoops 2018 TrialConsent® Hat Trick as CARE Award Finalist
CRF Health's TrialConsent (eConsent Solution) Shortlisted as Best Patient-Focused Technological Development in Clinical & Research Excellence Awards (CARE) Awards
Innovations in e-Consent: Reducing Regulatory Risk While Improving Participant Comprehension
As regulatory agencies push for more effective informed consent processes in clinical trials, eConsent can mitigate regulatory risk, while improving patient comprehension, compliance, and retention.
3 Major Regulatory Risks You Can Reduce with Electronic Informed Consent