PCMG Workshop: 

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

PANEL DISCUSSION
Innovative approaches with RW & Contracting
Tanja Wagner
Vice President, Evidence Strategy

Barbara Arone
Vice President, Medical Affairs Category Lead

Andrew Ecob
Senior Director, Head of Emerging Delivery Models

Kindly sponsored by IQVIA

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