The future regulation of artificial intelligence systems in healthcare services and medical research in the European Union by Janos Meszaros, Janos Meszaros, Jusaku Minari, Isabelle Huys, Isabelle Huys

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Digitizing the Informed Consent Process: A Review of the Regulatory Landscape in the European Union by Evelien De Sutter, Janos Meszaros, Pascal Borry, Isabelle Huys, Isabelle Huys

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Emerging Insights into European Markets of Biologics, Including Biosimilars by Steven Simoens, Isabelle Huys

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Innovative Approaches to Increase Access to Medicines in Developing Countries by Hilde Stevens, Isabelle Huys

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R&D Costs of New Medicines: A Landscape Analysis by Steven Simoens, Isabelle Huys

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Exploring new uses for existing drugs: innovative mechanisms to fund independent clinical research by Ciska Verbaanderd, Ilse Rooman, Isabelle Huys

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An overview of patents on therapeutic monoclonal antibodies in Europe: are they a hurdle to biosimilar market entry? by Evelien Moorkens, Arnold G. Vulto, Isabelle Huys

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Opportunities and Challenges in Cross-Country Collaboration: Insights from the Beneluxa Initiative by Zilke Claessens, Michiel Lammens, Liese Barbier, Isabelle Huys

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Past, Current, and Future Cancer Clinical Research Collaborations: The Case of the European Organisation for Research and Treatment of Cancer by Stefanie Broes, Robbe Saesen, Denis Lacombe, Isabelle Huys

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Methodological Quality Assessment of Budget Impact Analyses for Orphan Drugs: A Systematic Review by Khadidja Abdallah, Isabelle Huys, Kathleen Claes, Steven Simoens

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How to Value Orphan Drugs? A Review of European Value Assessment Frameworks by Alessandra Blonda, Yvonne Denier, Isabelle Huys, Steven Simoens

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Protection of Phage Applications in Crop Production: A Patent Landscape by Dominique Holtappels, Rob Lavigne, Isabelle Huys, Jeroen Wagemans

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Insights into European drug shortages: a survey of hospital pharmacists. by Kim Pauwels, Steven Simoens, Minne Casteels, Isabelle Huys

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Informing a European guidance framework on electronic informed consent in clinical research: a qualitative study by Evelien De Sutter, Pascal Borry, Isabelle Huys, Liese Barbier

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Personalized and long-term electronic informed consent in clinical research: stakeholder views by Evelien De Sutter, Pascal Borry, David Geerts, Isabelle Huys

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Developing a Methodology to Balance Benefit-Sharing: Application in the Context of Biodiversity Beyond National Jurisdiction by Jane Eva Collins, Aysegul Sirakaya, Thomas Vanagt, Isabelle Huys

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Time Investment in Drug Supply Problems by Flemish Community Pharmacies by Elfi De Weerdt, Steven Simoens, Minne Casteels, Isabelle Huys

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How Can We Optimize the Value Assessment and Appraisal of Orphan Drugs for Reimbursement Purposes? A Qualitative Interview Study Across European Countries by Alessandra Blonda, Yvonne Denier, Isabelle Huys, Pawel Kawalec, Steven Simoens

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Do European regulatory measures accelerate national market access in Belgium? A retrospective analysis of medicines centrally authorised between 2015 and 2020 by Isabelle Huys, Steffen Fieuws, Zilke Claessens, Joël Daems, Liese Barbier

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Stakeholder Perspectives on Access and Benefit-Sharing for Areas Beyond National Jurisdiction by Jane Eva Collins, Jane Eva Collins, Thomas Vanagt, Isabelle Huys

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