Webinar Recordings

  • Patient-Facing Technologies in Clinical Research: Myths vs. Reality1:00:56

    Patient-Facing Technologies in Clinical Research: Myths vs. Reality

    This webinar explores misconceptions surrounding technologies like eConsent and BYOD ePRO with industry experts, helping you make informed decisions and improve your clinical trial success.

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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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  • Improving Data Quality in Dermatology Clinical Trials59:07

    Improving Data Quality in Dermatology Clinical Trials

    This webinar discusses the unique data collection challenges faced by dermatology clinical trials and how they can be improved with eCOA, rater training and effective analytics.

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  • Improving Data Quality in Dermatology Clinical Trials59:07

    Improving Data Quality in Dermatology Clinical Trials

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  • Lessons Learned from the Clinical Trial Trenches: How to Use Patient Engagement Technology Successfully57:44

    Lessons Learned from the Clinical Trial Trenches: How to Use Patient Engagement Technology Successfully

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  • How Your Clinical Supply Chain Can Achieve Extended Enterprise Maturity58:24

    How Your Clinical Supply Chain Can Achieve Extended Enterprise Maturity

    This session will define four stages of clinical supply chain maturation and help you determine which stage your company is at today.

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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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  • 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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  • 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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  • Monitoring Considerations for Clinical Trials with eConsent1:01:36

    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.

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  • Monitoring Considerations for Clinical Trials with eConsent1:01:36

    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.

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  • 5 Best Practices for Using Connected Devices in Clinical Trials53:02

    5 Best Practices for Using Connected Devices in Clinical Trials

    Learn how you can use new technology in your clinical trials with remote patient monitoring, connected devices, and digital health tools.

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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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  • 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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  • 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.

    Watch Video
  • The World's Best eCOA Body Map: How Patients Helped Improve Symptom Location Reporting49:04

    The World's Best eCOA Body Map: How Patients Helped Improve Symptom Location Reporting

    The design of this eCOA body map was directed by the user experience of actual patients during the usability testing process. Improved symptom location reporting results in higher data quality.

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  • 6 Key Considerations for Complete Paper to eCOA Migration57:51

    6 Key Considerations for Complete Paper to eCOA Migration

    Migration of a clinical study from paper to electronic requires technical, regulatory, and patient experience considerations. Follow these best practices to ensure an effective transition to eCOA.

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