This webinar covers the various technical, logistical, cultural, linguistic, and regulatory challenges that may arise when deploying ePRO in certain geographic locations and ways to overcome them. We also review last month's survey results. Our guest presenter is Kristina Ernberg.
Home » Webinar Recordings » Deploying ePRO in Challenging Geographic Locations, Languages, and Cultures
Using Real-Time Reports in ePRO Studies to Better Manage Your Sites and Patients
Chris Clancy discusses real-time reports from ePRO data, demonstrating how specific reports will be of inte...
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.
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
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
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
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
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.
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
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
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.
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.
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.
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.
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
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
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
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