eConsent - Electronic Informed Consent

Learn all about the benefits of Electronic Informed Consent (eConsent) in our dedicated resource hub.

  • Using eConsent in Clinical Research to Support Patient Understanding and Welfare

    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.

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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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  • Translations and eConsent3:13

    Translations and eConsent

    When designing an informed consent, it's extremely important to consider the participants using it. Specifically, the consent should be created in a language that its primary audience will understand.

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  • eConsent: Five (5) Key Areas of Preparation

    eConsent: Five (5) Key Areas of Preparation

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  • CRF Health Launches TrialConsent™ 2.0 Platform

    CRF Health Launches TrialConsent™ 2.0 Platform

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  • TrialConsent™, An Electronic Informed Consent Solution2:54

    TrialConsent™, An Electronic Informed Consent Solution

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  • eConsent: Enabling the Patient-Centered Clinical Trial of Tomorrow, Today37:33

    eConsent: Enabling the Patient-Centered Clinical Trial of Tomorrow, Today

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  • Can Seniors Use eConsent?2:45

    Can Seniors Use eConsent?

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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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  • State of eConsent 2017 Report - Site Edition

    State of eConsent 2017 Report - Site Edition

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  • In Pursuit of eConsent: Best Practice Recommendations for Successful Integration

    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

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  • Recruitment & Retention: Breaking Down the Barriers to eConsent Adoption

    Recruitment & Retention: Breaking Down the Barriers to eConsent Adoption

    Provided by ACRP's Clinical Researcher Magazine. Original at https://www.acrpnet.org/2017/04/01/recruitment-retention-breaking-barriers-econsent-adoption/ For more information on electronic informed

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  • FDA Supports Innovation in Clinical Trials with eConsent4:12

    FDA Supports Innovation in Clinical Trials with eConsent

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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

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  • State of eConsent 2017 Report

    State of eConsent 2017 Report

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  • INFOGRAPHIC: 14 Drivers of eConsent Adoption in Clinical Trials

    INFOGRAPHIC: 14 Drivers of eConsent Adoption in Clinical Trials

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  • The Essential Guide to Electronic Informed Consent

    The Essential Guide to Electronic Informed Consent

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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

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  • Reducing Regulatory Risk with eConsent3:14

    Reducing Regulatory Risk with eConsent

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  • How eConsent Improves Consent Development 2:59

    How eConsent Improves Consent Development

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