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Square Brussels Convention Centre

Mar 12, 2024 9:00 AM - Mar 14, 2024 4:00 PM

Glass Entrance, Mont des Arts/Kunstberg, 1000 Brussels, Belgium

DIA Europe 2024

Live Oral Poster Presentations I

Session Chair(s)

Vedran   Raguz

Vedran Raguz

Scientific Programs Specialist

DIA, Switzerland

This session is an opportunity to hear Authors present their Posters Live, followed by a Q&A portion.

Learning Objective : The European Commission’s (EC) Pharmaceutical Strategy for Europe aimed to develop a future-proof pharmaceutical policy. This study aims to assess stakeholders' views on patient-centric policy initiatives and the prospects for patient-experience data (PED), expressed in the Pharmaceutical Strategy.

Speaker(s)

Io  Wens, MSc

Towards patient-centered pharmaceutical policy-making: Stakeholders’ perspectives on the Pharmaceutical Strategy for Europe

Io Wens, MSc

KU Leuven, Belgium

PhD Researcher

Anna  Litsiou, PhD, MBA, MSc

Sustainable Regulatory Framework: A toolkit of regulatory processes and tools to enable patient access and foster innovation

Anna Litsiou, PhD, MBA, MSc

AstraZeneca, United Kingdom

International Regulatory Affairs Policy And Intelligence

Alice  Vanneste, MS, MSc

Advancing Patient Experience Data in Healthcare Decision-Making: Multi-stakeholders’ insights on policy ways forward

Alice Vanneste, MS, MSc

KU Leuven, Belgium

PhD Student

Marjon  Pasmooij, PhD

Data science and artificial intelligence to study the drug regulatory system: current and future avenues

Marjon Pasmooij, PhD

Dutch Medicines Evaluation Board / Utrecht University, Netherlands

Head Science Department / Associate Professor of Drug Regulatory Science

Antoine  Manson, PharmD, MPharm

Using AI to Accelerate Medicines Development: An Evolving EU Regulatory Landscape

Antoine Manson, PharmD, MPharm

Bayer AG, France

Regulatory Policy and Innovation Specialist

Katelyn  Rivas, PhD

Lessons Learned: A Supplier’s Perspective on Strategies for Promoting Sustainability in the Regulatory Submissions Process

Katelyn Rivas, PhD

Synterex, Inc., United States

Regulatory Medical Writer

Daniel  Reed, PhD

Regulatory science considerations for cell and gene therapy in chronic diseases: cardiovascular disease as a case study

Daniel Reed, PhD

AstraZeneca, United Kingdom

Senior Regulatory Intelligence Director

Carolyn  Hynes, PhD

Access to Medicines: Models for future Regulatory Authority and HTA body work-sharing?

Carolyn Hynes, PhD

AstraZeneca, United Kingdom

Senior Director Regulatory Intelligence

Sevengul  Car, MS, MSc

Evolving Global Regulatory Landscape for Approval of Biosimilars: Current Challenges and Future Considerations

Sevengul Car, MS, MSc

KU Leuven, Belgium

PhD researcher

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