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Swissôtel Le Plaza

Oct 24, 2019 9:00 AM - Oct 25, 2019 5:30 PM

Messeplatz 25, 4005 Basel, Switzerland

Value, Access & Regulatory Evidence Workshop

Acknowledging the different perspectives and finding the pragmatic way forward

Session 2: Parallel Scientific Advice

Session Chair(s)

Anja  Schiel, PhD

Anja Schiel, PhD

Special Advisor, Lead Methodologist; Leader international HTA (iHTA) NoMA

Norwegian Medicines Agency (NoMA), Norway

In this session, the different Stakeholder experiences with Parallel Scientific Advice will be presented. The Speakers will reflect on their learnings as well as discuss how such learnings can translate into improvements that can be proposed for the future. This session also sets the scene for the SA role-play in session 3 where participants are encouraged to take different Stakeholder perspectives when discussing different theoretical products.

Speaker(s)

Michael  Berntgen, PhD

The Regulatory Perspective

Michael Berntgen, PhD

European Medicines Agency, Netherlands

Head of Scientific Evidence Generation

Anja  Schiel, PhD

HTA Body Perspective

Anja Schiel, PhD

Norwegian Medicines Agency (NoMA), Norway

Special Advisor, Lead Methodologist; Leader international HTA (iHTA) NoMA

Judith  Creba, PhD

The Industry Perspective, Pros and Cons

Judith Creba, PhD

Novartis Pharma AG, Switzerland

Sr. Global Program Regulatory Director, Reg Affairs GDD Region EU

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