This video goes over real-time reports from ePRO data, different users and roles in those reports, and the types of reports available throughout the study with ePRO. We also review last month's survey and introduce live-polling.
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CRF Health and University Hospital Basel Collaborate to Create Electronic Version of the Neurostatus-EDSSRead Case Study
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
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.
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
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
The World's Best eCOA Body Map: How Patients Helped Improve Symptom Location Reporting
6 Key Considerations for Complete Paper to eCOA Migration
3 Major Regulatory Risks You Can Reduce with Electronic Informed Consent
How to Calculate the True Cost of Paper When Considering eCOA
How to Visualize Data to Increase Trial Performance and Efficiencies
<p>Identifying hidden patterns in patient behavior can help you run an efficient and successful clinical trial. With powerful new visualization tools for reporting and analysis, CRF Health's TrialMan
SCDM Presents: Managing eCOA Data - Principles and Best Practices
<p>In this webinar, SCDM invites CRF Health to discuss the principles of managing eCOA data in clinical trials. We will use experience from real life studies to illustrate how to handle issues clinica
Innovations in e-Consent: Reducing Regulatory Risk While Improving Participant Comprehension
<p>Informed consent has a major impact on regulatory compliance, enrollment rates and expenses across the life of your study. Yet the traditional paper-based process has transformed informed consent i
eCOA Essentials: 1 Hour to Higher Quality Data
<p>The industry's shift from paper to electronic Clinical Outcome Assessments (eCOA) in clinical trials is happening at dizzying speeds.</p> <p>Trials that eliminate paper in favor of eCOA regularly
Winning Strategies for Successful eCOA Implementation
<p>An increasing number of clinical trials are using Electronic Clinical Outcome Assessments (eCOA) to capture more accurate patient data while creating a better trial experience for participants, sit
eCOA Design Like Nike: How a Great Interface Can Improve the Clinical Trial Experience
<p>Nike is one of the most valuable brands in the world, attributed to a deep knowledge of its customers and the design of products which fit their needs: aesthetically, functionally and emotionally.<
Paper: No Longer the Gold Standard of Data Capture in Clinical Trials
<p>Clinical Trials have traditionally collected data from patients by using the most ubiquitous technology of all: the pen and paper. While the use of electronic patient reported outcomes (ePROs) is b
Translation of eCOA in Global Studies: Challenges and Solutions
What Metadata Can Teach Us About Actual Patient Reporting Behavior
eCOA and Equivalence Testing: New Evidence from Meta-Analysis
Usability Testing of electronic Patient Reported Outcomes (ePRO)