Error - something went wrong!
Other content in this Stream
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.
Managing eCOA Data - Principles and Best Practices
9 KPI Dashboards & Reports No eCOA Study Should Be Without
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.
Developing an eCOA Device Supply Strategy: The Vital Considerations for a Global Clinical Trial
With the increasing complexities of today's clinical trials, including the ever-rising number of studies spanning numerous continents and sites, managing the cost of a global trial can prove challen
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.
The Shocking Truth About Paper Backups in eCOA Studies
While paper has long been the trusted system for clinical trial backup, a recent study reveals the medium does carry risk. Learn how eCOA can mitigate risk and relieve the burden of managing paper.
The Challenges of Paper Backups in eCOA Studies
Effective ePRO Training Increases Patient Compliance
Brought to your by CRF Health and the TrialMax eCOA Solution - visit www.crfhealth.com for more information
PROs and Your Clinical Trial: Choosing, Administering, and Claiming
Measuring Patient ePRO Burden Through Completion Times
Rob Arbuckle, Chloe Tolley, and Karl McEvoy present research findings related to diary completion times in clinical trials, suggesting best practices for reducing patient burden with ePRO solutions.
Integrating Today's eCOA Solutions Intelligently and Efficiently
Keith Wenzel and Rauha Tulkki-Wilke draw on case studies to give review the current electronic data gathering environment and identify best practices for eCOA integration into clinical studies.
Overcoming Logistical Challenges in Global Clinical Trials
Deploying eCOA in a global clinical study requires a reliable supply chain, as well as an understanding of trade protocols for individual countries as they relate to importation of electronic devices.
Successful Management of eCOA Data
Chapter 2 of a two-part series, providing an overview of electronic data collection. Nora Ibrahimova covers best practices for implementation of eCOA and management of real-time assessment data.
Clinical Outcome Assessments and Your Study
Andrea Murison of Mapi Research Trust joins Paul O’Donohoe to discuss considerations and resources for selecting clinical outcome assessments for a clinical trial and discuss adaptation to electronic.
Which ePRO Solution is Right for your Study? (I)
Part 2 of 2: Robyn Carson, Elsie Mathews, and John Jordan discuss various types of ePRO and outline considerations for selecting an appropriate mode for a clinical study. Recorded January 20, 2011.
For CROs: ePRO Best Practices - Part I
Part 1 of 2: Gregg Jewett discusses the state of the clinical trials industry, outlining benefits and best practices for CROS and sponsors within a CRO-ePRO partnership. Recorded March 17, 2011.
For CROs: ePRO Best Practices - Part II
Part 2 of 2: An overview of benefits and best practices for CRO-ePRO partnerships with particular focus on business development, operations and delivery, and data management. Recorded April 21, 2011.
How to Realize Time and Cost Savings by Standardizing ePRO Deployment