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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

Io Wens, MSC

PhD Researcher, KU Leuven University, Belgium

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

Anna  Litsiou, PHD, MBA, MSC

Anna Litsiou, PHD, MBA, MSC

Regulatory Policy & Intelligence Director, AstraZeneca, United Kingdom

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

Alice  Vanneste, MSC

Alice Vanneste, MSC

PhD Student, KU Leuven, Belgium

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

Marjon  Pasmooij, PHD

Marjon Pasmooij, PHD

Head Science Department, MEB, Netherlands

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

Antoine  Manson, PHARMD, MPHARM, MS

Antoine Manson, PHARMD, MPHARM, MS

Senior Manager, Regulatory Policy and Science, Bayer, United States

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

Katelyn  Rivas, PHD

Katelyn Rivas, PHD

Regulatory Medical Writer, Synterex, Inc., United States

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

Dan  Reed, PHD

Dan Reed, PHD

Senior Regulatory Intelligence Director, AstraZeneca, United Kingdom

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

Carolyn  Hynes, PHD

Carolyn Hynes, PHD

Senior Director Regulatory Intelligence, AstraZeneca, United Kingdom

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

Sevengul  Car, MS, MSC

Sevengul Car, MS, MSC

PhD researcher, KU Leuven, Belgium

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

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