Real world evidence: New ways of thinking, better study delivery models
PCMG have invited IQVIA to join this VIRTUAL event to shine a light on the realities of RWE and it’s application in the real world of outsourced clinical trials. This online event will include:
Open discussion of the fundamentals of RWE
What are the latest innovations in RWE application and clinical trial design options
Changes in regulatory landscape and the growing acceptance of RWE at a global level.
Managing the risk of RWE inclusion in regulatory submissions and the use of early engagement
Panel discussion on selecting RWE services including
External comparators
Enriched trials
Direct-to-patient and virtual approaches
The shift from primary data collection to secondary data use and re-use
Contracting structures
PROGRAMME
WELCOME AND INTRODUCTION
PRESENTATION Innovative Approaches to Generate RWE
Andrea Spannheimer
SrVP, Global Head of RWS Offerings, Innovations and Partnerships
PRESENTATION Regulatory Bodies and the Use of RWE for Decision-making
Matthew W. Reynolds, PhD, FISPE
Vice President, Real World Evidence