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Virtual

Nov 15, 2023 1:00 PM - Nov 16, 2023 6:40 PM

DIA Innovating Clinical Trials in Europe

This year's must-attend virtual live conference for pharmaceutical innovators and clinical researchers alike!

Session 7: Part II: Real-World Evidence in Regulatory and HTA Decision-Making: Global and Regional Perspectives on Moving from Pilots to Operation

Session Chair(s)

Álmath  Spooner, PhD

Álmath Spooner, PhD

Head of Europe Regulatory Policy & Intelligence (RPI)

Abbvie, Ireland

Lembit  Rago, DrMed, MD, PhD

Lembit Rago, DrMed, MD, PhD

Secretary General

Council for International Organizations of Medical Sciences (CIOMS), Switzerland

This session will aim to showcase the draft report and review that has been undertaken by CIOMS and EMA, respectively, into the application of real-world evidence. We will attempt to tease out critical success factors in delivering RWD/E for multiple stakeholders’ needs. The use of real-world data and real-world evidence in regulatory and HTA decision making has been under discussion for more than a decade. However, where it would have been a novelty several years ago, it is now playing an increasingly significant role through early to late-stage drug development and in regulatory and market access decisions. This is observed in the context of rare and orphan disease and other unique patient populations such as children and women of child-bearing age (WOCBA), but it is also of relevance for broader patient populations, particularly where there is a need to demonstrate efficacy and effectiveness in the longer term.

Speaker(s)

Álmath  Spooner, PhD

Introduction to the session

Álmath Spooner, PhD

Abbvie, Ireland

Head of Europe Regulatory Policy & Intelligence (RPI)

Lembit  Rago, DrMed, MD, PhD

Introduction and Background to CIOMS Draft Report

Lembit Rago, DrMed, MD, PhD

Council for International Organizations of Medical Sciences (CIOMS), Switzerland

Secretary General

Gracy G Crane, PhD, MS

Global and regional harmonization initiatives relating to RWE

Gracy G Crane, PhD, MS

Roche, United Kingdom

Policy Lead

Stefanie  Prilla, DrSc

Regulator-led RWE Studies – an EMA Review of the Experience Gained

Stefanie Prilla, DrSc

European Medicines Agency, Netherlands

RWE Coordinator

Daniel   Prieto-Alhambra

Executing Real-World Studies – Use Case

Daniel Prieto-Alhambra

and Professor at University of Oxford and Erasmus MC, United Kingdom

Section Head - Health Data Sciences at Botnar Research Centre

Elena  Petelos

Application of RWE in HTA decision-making: use case

Elena Petelos

University of Maastricht, HTAi, Netherlands

Lecturer of Evidence-Based Medicine and Evidence-Informed Policy

Estelle  Michael

Panel Discussion: Real world evidence in regulatory decision making – critical success factors?

Estelle Michael

UCB, Belgium

RWE Policy & External Engagement Lead

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