Upcoming ePRO Webinars
- Session 21: Thursday, September 16, 2010 11:00 a.m. EDT (1 hour)
Topic: Using Real-Time Reports in ePRO Studies to Better Manage your Sites and Patients
- Session 22: Thursday, October 21, 2010 11:00 a.m. EDT (1 hour)
Topic: Deploying ePRO in Challenging Geographic Locations, Languages, and Cultures
- Session 23: Thursday, November 18, 2010 11:00 a.m. EDT (1 hour)
Topic: Archiving ePRO Data: What to Expect in your Electronic Source Data Archives
- Session 24: Thursday, December 16, 2010 11:00 a.m. EDT (1 hour)
Topic: Web-Diary
Previously Recorded ePRO Webinars
- Session 1: January: ePRO Deployment Basics
- Session 2: February: Integration of ePRO with Medication Management Using
a Barcode Scanner
- Session 3: March: Reminders - Alerts & Other Mechanisms to
Promote Maximum Patient Compliance
- Session 4: April: Deployment to India / Japan and Other Challenging Places
- Session 5: May: Instrument Validation, Psychometric Testing Including a Discussion of FDA Guidance and ISPOR
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Session 6: June: ePRO Discrepancy Management - How to Efficiently Clean ePRO Data and Resolve Discrepancies
- Session 7: July: Tips for Successful Translation & Localization of ePRO Applications for Global Studies
- Session 8: August: The Importance of Web-Based, Real-Time Reports for Global ePRO Projects
- Session 9: September: The Advantages of ePRO For Pain Studies
- Session 10: October: Helpdesk Support for Sites, Subjects, and Sponsor Teams for Global ePRO Deployment
- Session 11: November: Making the Transition from Paper to ePRO: An Industry Perspective
- Europe Session 1: The Value Proposition of ePRO Compared to Paper PRO
- Session 12: December: ePRO Benefits and Burdens from the Site Perspective
- Session 13: January 2010: Industry Perspectives on the Final PRO Guidance Document Focusing on ePRO: Are there any eCONS?
- Session 14: February: The Value Proposition of ePRO Compared to Paper PRO
- Session 15: March: A Better View: Integrating ePRO and EDC for More Comprehensive Patient Data
- Session 16: April: FDA PRO Guidance Compliance: Practical PRO/ePRO Instrument Equivalence Tips
- Session 17: May: ePRO Devices - Practical and Regulatory Considerations
- Session 18: June: Back to Basics: ePRO Basics & Fundamentals
- Session 19: July: ePRO Design and Implementation: What to Expect During the Design of an ePRO Solution for Your Project
- Session 20: August: How to Maximize Patient Comliance Using ePRO
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