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ePRO Webinar Series by CRF Health - Join Us!

CRF Health ePRO Webinar Series

Sign up for the CRF Health Monthly Webinar Series to hear about the latest industry trends and developments in ePRO.

Click Here to Register For This Month's Webinar

Recordings of the previous webinar sessions are available now in a self-paced web-enabled format. Please send an email to crf-info@crfhealth.com with WEBINAR ARCHIVE in the subject line.

Below is a listing of our upcoming ePRO webinars and previously recorded sessions.

   

Upcoming ePRO Webinars

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

  • 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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