Webinar Recordings

Binge watch these on-demand webinars with key eConsent subject matter experts.

  • Monitoring Clinical Trials with Electronic Informed Consent1:01:36

    Monitoring Clinical Trials with Electronic Informed Consent

    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.

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  • Electronic Informed Consent - 2017 Industry Survey Results from Clinical Sites1:02:32

    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.

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  • Electronic Informed Consent: 2017 Industry Survey Results55:21

    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.

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  • Visibility and Oversight: What Paper Informed Consent Isn't Offering You58:03

    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.

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  • Innovations in e-Consent: Reducing Regulatory Risk While Improving Participant Comprehension1:00:01

    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.

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  • 3 Major Regulatory Risks You Can Reduce with Electronic Informed Consent54:25

    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.

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