CRF Health - eCOA and eConsent Resource Hub

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Home » Webinar Recordings » ePRO Deployment Basics

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ePRO Deployment Basics

March 23, 2015

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Recorded live June 17, 2010

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ePRO Devices: Practical and Regulatory Considerations

ePRO Devices: Practical and Regulatory Considerations

John Hutchin discusses current ePRO device technologies, highlighting practical and regulatory consideratio...

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ePRO Design and Implementation: What to Expect During the Design of an ePRO Solution

ePRO Design and Implementation: What to Expect During the Design of an ePRO Solution

Chris Clancy gives a guide to the process of preparing for an ePRO clinical study, using a week-by-week des...

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1:01:36

Monitoring Clinical Trials with Electronic Informed Consent

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 Trials

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

Electronic Informed Consent - 2017 Industry Survey Results from Clinical Sites

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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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1:02:21

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.

Electronic Informed Consent: 2017 Industry Survey Results

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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.

Visibility and Oversight: What Paper Informed Consent Isn't Offering You

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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.

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

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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.

6 Key Considerations for Complete Paper to eCOA Migration

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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.

3 Major Regulatory Risks You Can Reduce with Electronic Informed Consent

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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 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.

How to Visualize Data to Increase Trial Performance and Efficiencies

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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.

SCDM Presents: Managing eCOA Data - Principles and Best Practices

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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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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 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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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 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.

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

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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.

Translation of eCOA in Global Studies: Challenges and Solutions

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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.

What Metadata Can Teach Us About Actual Patient Reporting Behavior

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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.

eCOA and Equivalence Testing: New Evidence from Meta-Analysis

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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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