Binge watch these on-demand webinars with key eConsent subject matter experts.
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.
Monitoring Considerations for Clinical Trials with eConsent
During this webinar, informed consent experts with decades of hands-on monitoring experience discuss the challenges they’ve encountered and how to overcome them with the integration of eConsent.
Electronic Informed Consent - 2017 Industry Survey Results from Clinical Sites
In this webinar, CRF Health's Sandra "SAM" Sather is joined by Giga Smith from Coastal Carolina Healthcare (CCHC) to discuss Electronic Informed Consent (eConsent) from the research site perspective.
Electronic Informed Consent: 2017 Industry Survey Results
Sam Sather, Regulatory & Quality Lead for TrialConsent™, discusses survey findings from the State of eConsent 2017 Report. Find out why 82% of pharma companies are projected to adopt eConsent by 2020.
Visibility 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.
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
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.