Events

European Medicines Agency focus on availability and access of medicines

How are we gearing up to the challenges?

Thursday, 28 September 2023 | 10:15-11:30 | Conference Centre

Organised by the European Medicines Agency

The New Pharmaceutical legislation sets out ways to increase availability, access and affordability of medicines (“triple A”).

The European Medicines Agency is already actively implementing the Regulatory Science Strategy and European Medicines Regulatory Network Strategy to 2025. These strategies address the triple A challenge, with increased dialogue with patients and healthcare professionals, HTA and payers, as well as embracing new technologies, influencing and facilitating development of highly innovative medicines and treatment.

Join us for this session to debate with key stakeholders whether regulators are on the right track with the strategies they have set out to enable access and availability of medicines. Share your view on opportunities arising from current significant changes in the European ecosystem and anticipating the impact of the “triple A” political objectives in the new pharma legislation. Debate with us what success looks like in delivering on those!

Session Recording

Speakers & panellists

SPEAKERS

  • Michael Berntgen, Head of the Scientific Evidence Generation Department, European Medicines Agency
  • Marcus Guardian, Chief Operating Officer, European Network for Health Technology Assessment
  • Annika Tibell, Director of Research, Development, Education, and Innovation, Karolinska University Hospital
  • Virginie Hivert, Therapeutic Development Director, EURORDIS
  • Michael Zaiac, Head of Medical Affairs Oncology Europe and Canada, Daiichi Sankyo

MODERATED BY

  • Anthony Humphreys, Head, Regulatory Science and Innovation Taskforce, European Medicines Agency

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