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Event
Session 41 - March 1, 2012
The Biotech Essential Guide to ePRO: Benefits of Partnership Between CROs &
ePRO Providers
Guest Speakers:
Chris Clancy, Director of Business Development, CRF Health
Christine Kanalis,
Manager Data Management, PRA
Session 40 - February 23, 2012
Back to Basics: ePRO Basics & Fundamentals
Guest Speakers:
Jane Carter, Program Manager, CRF Health
Session 39 - Archive from January 19, 2012
Clinical Outcome Assessments: Considerations in Migration and Validation
Guest Speakers:
Kai Langel, Senior Director, Technical Support, CRF Health
Diane Wild, VP, ePRO and Translations, Oxford Outcomes
Session 38 - Archive from December 15, 2011
The Benefits of
Web-Based ePRO for Phase IV Clinical Studies
Guest Speakers:
Rauha Tulkki-Wilke, Director,
Product Management, CRF Health
Session 37 - Archive from November 22, 2011
Detecting
Pro-Cognitive Effects in Clinical Drug Trials: Case Studies from Alzheimer’s
Disease
Guest Speakers:
Dr. John Harrison, Scientific Consultant, CRF Health
Session 36 - Archive from October 20, 2011
Efficient
Integration of ePRO and Other eClinical Systems for the Benefit of Clinical
Studies
Guest Speakers:
Pekka Keskiivari, CTO, CRF Health
Rauha Tulkki-Wilke, Director, Product Management, CRF Health
Session 35 - September 29, 2011, 10AM BST
Efficient
Integration of ePRO and Other eClinical Systems for the Benefit of Clinical
Studies
Guest Speakers:
Pekka Keskiivari, CTO, CRF Health
Rauha Tulkki-Wilke, Director, Product Management, CRF Health
Session 34 - Archive from September 15, 2011
Multiple Sclerosis Clinical Trials - ePRO and eClinRO Best Practices
Guest Speakers:
Kai Langel, Senior Director, Technical Support, CRF Health
Glenn Gammer, Project Manager, CRF Health
Session 33 - Archive from August 18, 2011
Compliance in Challenging Patient Populations and the Role of the Caregiver
Guest Speakers:
Kai Langel, Senior Director, Technical Support, CRF Health
Rohini Beavon, PhD, Director of R Beavon Solutions Limited
Session 32 - Archive from July 21, 2011
How to Standardize and Scale Up ePRO Deployments
Guest Speakers:
Debi Maloney, VP Corporate Accounts, CRF Health
Martin Grant, Program Manager, CRF Health
Session 31 - Archive from June 16, 2011
Considerations for the Use of eDiaries in Parksinson's Disease Clinical Trials
Guest Speakers:
Kai Langel, Senior Director Technical Support, CRF Health
Robert Hauser, MD, USF Parkinson's Disease & Movement Disorders Center
Session 30 - May 19, 2011
The Patient
Perspective: Feedback/Opinions on Various ePRO Modalities
Guest Speakers:
Rauha Tulkki-Wilke, Director Product Management, CRF
Health
Sarah Hearn, Associate Outcomes Researcher, Oxford Outcomes
Session 29 - Archive from April 21, 2011
CRO ePRO Delivery:
Best Practices - Part 2
Guest Speakers:
Gregg Jewett, Senior Director, Strategic Alliances and
Partnerships, CRF Health
Session 28 - Archive from March 17, 2011
CRO ePRO Delivery:
Best Practices - Part 1
Guest Speakers:
Gregg Jewett, Senior Director, Strategic Alliances and Partnerships,
CRF Health
Session 27 - Archive from February 16, 2011
Generating the
Evidence Required for Content Validity
Guest Speakers:
Bonnie Teschendorf, PhD, PRO
Scientific Advisor, CRF Health
Session 25 - Archive from January 20, 2011
Which ePRO
Solution is Right for Your Study? Bringing Clarity to ePRO Choices Part 2:
ePRO via SMS, Web, or Phone? Which is Right for Your Clinical Study?
Guest Speakers:
John Jordan, Sr. VP of eClinical Technologies
Elsie Matthews, Director, Data
Operations, Bristol-Myers Squibb
Robyn Carson, Assistant Director, Health Economics and Outcomes Research, Forest
Laboratories
Session 24 - Archive from December 16, 2010
Which ePRO Solution is Right for Your Study? Bringing Clarity to ePRO Choices Part 1: Home Based & Site Based ePRO Solutions are Examined
Guest Speakers:
John Jordan, Sr. VP of eClinical Technologies, CRF Health
Greg Burgess, Manager, External Data Acquisition Operations, Merck
Marianne Ciarricco, Assistant Director, Global Data Management and Standards, Merck
Session 23 - Archive from November 18, 2010
Back to Basics: ePRO Basics & Fundamentals
Guest Speakers:
- Jane Carter, Program Manager, CRF Health
Session 22
- Archive from October 21, 2010
Deploying ePRO in
Challenging Geographic Locations, Languages, and Cultures
Guest Speakers:
- Kristina Ernberg
Session 21
- Archive from September 16, 2010
Using
Real-Time Reports in ePRO Studies to Better Manage your Sites and Patients
Guest Speakers:
-
Chris Clancy, Director, Business Deveolpment
Session 20 -
Archive from August 19, 2010
How to
Maximize Patient Compliance Using ePRO
Guest Speakers:
-
Kai Langel, Systems Specialist
Session 19 -
Archive from July 15, 2010
ePRO
Design and Implementation: What to expect during the design of an ePRO
Solution for your project
Guest Speakers:
-
Chris Clancy, Director, Account Management
Session 18 -
Archive from June 17, 2010
Back to Basics: ePRO Benefits and Fundamentals
Guest Speakers:
-
Chris Clancy, Director, Business Development
Session 17 -
Archive from May 20, 2010
ePRO Devices - Practical and Regulatory Considerations
Guest Speakers:
-
John Hutchin, Director, Technical Support
Session 16 -
Archive from April 15, 2010:
Pro
Guidance Compliance: Practical PRO/ePRO Instrument Equivalence Tips
Guest Speakers:
-
Dian Wilde, Director, Oxford Outcomes
- Kai Langel, Senior Systems Specialist, CRF Health
Session 15 -
Archive from March 18, 2010:
EDC and ePRO Integration
Guest Speakers:
-
Joe Dustin, Business Consultant, Medidata
- John Hutchin, Senior Systems Specialist, CRF Health
Session 14 -
Archive from February 18, 2010:
The Value Proposition of ePRO Compared to Paper PRO
Guest Speakers:
-
Chris Clancy, Director of Business Development, CRF Health
- Kai Langel, Senior Systems Specialist, CRF Health
Session 13 -
Archive from January 21, 2010:
What the final FDA PRO guidance means for both US and EU clients
Guest Speakers:
-
John Jordan, COO, CRF Health
-
John Hutchin, Senior Systems Specialist, CRF Health
Session 12 -
Archive from December 17, 2009:
ePRO Benefits and Burdens from the SIte Perspective
Guest Speakers:
-
Nadina Jose, MD, Clinical Advisor, CRF Health
-
Christine Pierre, RN, CEO of RX Trials
-
Richard Beyerlein, MD, CPI CEO of
Clinical Trials of America
EU ePRO Webinar
- Archive from December 8, 2009
Value Proposition
of ePRO Compared to Paper PRO
Guest Speakers:
- Kai Langel,
Senior Systems Specialist,
CRF Health
- Sharon Kalewski, Director of Business Development, CRF Health
Session 11 -
Archive from November 19, 2009:
Making the Transition from Paper to ePRO: An Industry Perspective
Guest Speakers:
-
Mary Briggs, VP Global Sales & Marketing, CRF Health
-
John Jordan, Chief Operating Officer, CRF Health
-
Stefanie Alfano, Manager, GCDM, Schering-Plough Research Institute
-
Anna Maria Craun, Manager, Clinical Operations, Cephalon Inc
Session 10 - Archive from October 15, 2009 Event.
Helpdesk support for sites, subjects, and sponsor teams for global ePRO deployment
Session 9 -
Archive from September 17th, 2009 Event.
The value proposition of ePRO compared to paper PRO
Session 8 -
Archive from August 20, 2009 Event.
The importance of web-based, real-time reports for global ePRO projects
