eConsent

  • The University of Bristol Selects Signant Health's TrialConsent Solution in Oncology Trial

    The University of Bristol Selects Signant Health's TrialConsent Solution in Oncology Trial

    The Prestigious UK Academic Institution selected TrialConsent® to Administer eConsent to Benefit Sites and Patients in Future Clinical Research.

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  • Choose Wisely
  • Signant Selected as eConsent Provider by Shanghai Mental Health Center

    Signant Selected as eConsent Provider by Shanghai Mental Health Center

    Signant Health has been selected to provide eConsent for a significant neuroscience study by the prestigious Shanghai Mental Health Center (SMHC).

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  • TrialConsent Product Overview 2019

    TrialConsent Product Overview 2019

    Introducing an eConsent solution that makes digitizing the consent process easy at any scale. Use TrialConsent® on your next small study, complex study, or even virtual study.

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  • The Essential Guide to Electronic Informed Consent

    The Essential Guide to Electronic Informed Consent

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  • TrialConsent Self-Service and its Enablement

    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.

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  • TrialConsent for IRBs and ECs (Ethics Committees)

    TrialConsent for IRBs and ECs (Ethics Committees)

    Discover the value of TrialConsent (eConsent) for IRBs and Ethics Committees by Signant Health.

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  • 14 Drivers of eConsent Adoption

    14 Drivers of eConsent Adoption

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  • Signant Health Partner Program

    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.

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  • Enabling Electronic Informed Consent for Clinical Research Sites43:15

    Enabling 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.

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  • eConsent in Action - How It Works and Why Patients Appreciate It55:30

    eConsent 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.

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  • Optimizing eConsent for Patient Centricity1:01:23

    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.

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  • CRF Health Looks To Simplify eConsent For Both The Patient And The Researcher

    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.

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  • The Top 10 Myths of Electronic Informed Consent

    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.

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  • Preparing for eConsent - A Step by Step Guide for Site Personnel

    Preparing for eConsent - A Step by Step Guide for Site Personnel

    5 steps to help sites prepare for implementing an electronic informed consent (eConsent) solution.

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

    Recruitment & Retention: Breaking Down the Barriers to eConsent Adoption

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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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  • eConsent: Five (5) Key Areas of Preparation

    eConsent: Five (5) Key Areas of Preparation

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  • 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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  • CRF Health Scoops 2018 TrialConsent® Hat Trick as CARE Award Finalist

    CRF Health Scoops 2018 TrialConsent® Hat Trick as CARE Award Finalist

    CRF Health's TrialConsent (eConsent Solution) Shortlisted as Best Patient-Focused Technological Development in Clinical & Research Excellence Awards (CARE) Awards

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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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