Webinar Recordings

  • 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.

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  • 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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  • 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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  • How to Calculate the True Cost of Paper When Considering eCOA47:28

    How to Calculate the True Cost of Paper When Considering eCOA

    Some clinical trial sponsors fear the cost of eCOA will be prohibitive. We unpack the expense of paper data capture and compare it with the cost, and potential value benefits, of electronic modes.

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  • How to Visualize Data to Increase Trial Performance and Efficiencies48:54

    How to Visualize Data to Increase Trial Performance and Efficiencies

    This live demo shows how new visualization tools in CRF Health’s TrialManager 6.0 enable monitoring of patients and sites in real time, resulting in lower clinical trial costs and higher data quality.

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  • SCDM Presents: Managing eCOA Data - Principles and Best Practices1:04:19

    SCDM Presents: Managing eCOA Data - Principles and Best Practices

    At the invitation of SCDM, CRF Health reveals common issues related to data management. Presenters draw on real-life eCOA clinical studies to outline best practices for achieving high data quality.

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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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  • eCOA Essentials: 1 Hour to Higher Quality Data54:47

    eCOA Essentials: 1 Hour to Higher Quality Data

    This high-level introduction to electronic clinical outcome assessments will outline the many benefits of eCOA. Find out why the pharma research industry is rapidly shifting from paper to eCOA.

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  • Winning Strategies for Successful eCOA Implementation56:57

    Winning Strategies for Successful eCOA Implementation

    Drawing on 20+ years of experience in clinical research and ePRO/eCOA implementation, Scottie Kern provides strategies to ensure smooth implementation and widespread adoption of eCOA in your trials.

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  • eCOA Design Like Nike: How a Great Interface Can Improve the Clinical Trial Experience53:25

    eCOA Design Like Nike: How a Great Interface Can Improve the Clinical Trial Experience

    Paul Margerison demonstrates how principles of user experience design, used by companies like Nike, can be applied to eCOA to improve patient recruitment, compliance, and retention in clinical trials.

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  • Paper: No Longer the Gold Standard of Data Capture in Clinical Trials59:52

    Paper: No Longer the Gold Standard of Data Capture in Clinical Trials

    As the benefits of eCOA are positioning it as the preferred method of data capture in clinical trials, the industry has yet to realize the full potential of shifting from paper as its standard mode.

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  • Translation of eCOA in Global Studies: Challenges and Solutions1:01:30

    Translation of eCOA in Global Studies: Challenges and Solutions

    For global clinical trials, eCOA instruments must be translated and then validated. This webinar provides insight into the regulations, timelines, and best practices related to linguistic validation.

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  • What Metadata Can Teach Us About Actual Patient Reporting Behavior46:59

    What Metadata Can Teach Us About Actual Patient Reporting Behavior

    Anders Mortin of TriTiCon presents research findings on patient compliance in long-term clinical trials. Learn how eCOA metadata can help you identify patient reporting behaviours and preferences.

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  • eCOA and Equivalence Testing: New Evidence from Meta-Analysis1:05:23

    eCOA and Equivalence Testing: New Evidence from Meta-Analysis

    Is equivalence testing necessary to establish comparability between electronic and paper-based clinical trial questionnaires? A meta-analysis of several years of equivalence tests provides insights.

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  • Usability Testing of electronic Patient Reported Outcomes (ePRO)1:40:33

    Usability Testing of electronic Patient Reported Outcomes (ePRO)

    Members of Mapi Group join CRF Health to explain what usability testing is, and what it is not, in the context of ePRO. Presenters draw on real-life usability tests to provide tips for developing UT.

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