Our Latest Resources

  • 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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  • eConsent Webinar: About Our Speakers

    eConsent Webinar: About Our Speakers

    Learn more about speakers Sandra "SAM" Sather and Giga Smith, presenters of our upcoming webinar: Electronic Informed Consent: 2017 Industry Survey Results from Clinical Sites.

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  • Webinar: 5 Best Practices for Using Connected Devices in Clinical Trials

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  • How to Select Most Effective eCOA Modality for Your Study1:02:21

    How to Select Most Effective eCOA Modality for Your Study

    This webinar examines the electronic Clinical Outcome Assessment (eCOA) modalities available to clinical trials, such as handheld, tablet, web, Bring Your Own Device (BYOD), and mixed mode devices.

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  • Customer Insights

    Customer Insights
  • 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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  • 3 Protocol Considerations that Drive eCOA Design2:34

    3 Protocol Considerations that Drive eCOA Design

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  • eConsent: Five (5) Key Areas of Preparation

    eConsent: Five (5) Key Areas of Preparation

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  • 9 Key Factors to Evaluate When Considering BYOD

    9 Key Factors to Evaluate When Considering BYOD

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  • CRF Health Newsroom

    Latest News
  • DIA 2017 Recap: Wheel of Prizes at CRF Health Booth 2006

    DIA 2017 Recap: Wheel of Prizes at CRF Health Booth 2006

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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 Electronic Clinical Outcome Assessments (eCOA)?2:05

    Can Seniors Use Electronic Clinical Outcome Assessments (eCOA)?

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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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  • eCOA Value: Cost Savings and Beyond3:28

    eCOA Value: Cost Savings and Beyond

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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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  • Managing eCOA Data - Principles and Best Practices

    Managing eCOA Data - Principles and Best Practices

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  • TrialMax Slate Reduces Site Burden Conducting 6-Minute Walk Test

    TrialMax Slate Reduces Site Burden Conducting 6-Minute Walk Test

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