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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.

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
  • Session 21: September: Using Real-Time Reports in ePRO Studies to Better Manage Your Sites & Patients
  • Session 22: October: Deploying ePRO in Challenging Geographic Locations, Languages, and Cultures
  • Session 23: November: Back to Basics: ePRO Basics & Fundamentals
  • Session 24: December: Which ePRO Solution is Right for Your Study?  Bringing Clarity to ePRO Choices
    Part 1: Home Based & Site Based ePRO Solutions are Examined
  • Session 25: January 2011: Which ePRO Solution is Right for Your Study?  Bringing Clarity to ePRO Choices
    Part 2: ePRO Via SMS, Web, or Phone
  • Session 27: February 2011: Generating the Evidence Required for Content Validity
  • Session 28: March 2011: CRO ePRO Delivery: Best Practices, Part I
  • Session 29: April 2011: CRO ePRO Delivery: Best Practices, Part II
  • Session 30: May 2011: The Patient Perspective:  Feedback/Opinions on Various ePRO Modalities
  • Session 31: June 2011: Considerations for the Use of eDiaries in Parkinson's Disease Clinical Trials
  • Session 32: July 2011: How to Realize Time and Cost Savings By Standardizing ePRO Deployment
  • Session 33: August 2011: Compliance in Challenging Patient Populations and the Role of the Caregiver
  • Session 34: September 2011: Multiple Sclerosis Clinical Trials - ePRO and eClinRO Best Practices
  • Session 35 (EU): September 2011: Efficient Integration of ePRO and Other eClinical Systems for the Benefit of Clinical Studies
  • Session 36: October 2011: Efficient Integration of ePRO and Other eClinical Systems for the Benefit of Clinical Studies
  • Session 37: November 2011: Detecting Pro-Cognitive Effects in Clinical Drug Trials: Case Studies from Alzheimer’s Disease
  • Session 38: December 2011: The Benefits of Web-Based ePRO for Phase IV Clinical Studies
  • Session 39: January 2012: Clinical Outcome Assessments: Considerations in Migration & Validation
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