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TrialConsent for IRBs and ECs (Ethics Committees)
Discover the value of TrialConsent (eConsent) for IRBs and Ethics Committees by Signant Health.
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.
43:15Enabling 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.
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.
55:30eConsent 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.
1:01:23Optimizing 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.
5 steps to help sites prepare for implementing an electronic informed consent (eConsent) solution.
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
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's TrialConsent (eConsent Solution) Shortlisted as Best Patient-Focused Technological Development in Clinical & Research Excellence Awards (CARE) Awards
1:00:01Innovations 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.
54:253 Major Regulatory Risks You Can Reduce with Electronic Informed Consent
Does your clinical trial’s informed consent process stand up under regulatory scrutiny? Learn how eConsent can help to mitigate such risks as approval delay, fines, litigation, even trial failure.
58:03Visibility and Oversight: What Paper Informed Consent Isn't Offering You
Speakers from Chesapeake IRB and CRF Health discuss informed consent oversight and visibility. See how electronic informed consent (eConsent) enables top pharma companies achieve greater transparency.
55:21Electronic Informed Consent: 2017 Industry Survey Results