ISPOR Europe 2026
- Start Date:
08 Nov 2026
- End Date:
11 Nov 2026
- Location:
Vienna, Austria
- Booth #:
511
Evidence designed for access and built for the decisions ahead
Meet us at ISPOR Europe 2026
Meet our experts at ISPOR Europe 2026 to explore how integrated evidence strategies can help you prepare for the decisions that shape successful market access. From evolving HTA and payer requirements to the growing role of real-world evidence and AI, discover how designing the right evidence earlier can help demonstrate value across markets, navigate changing evidence expectations, and ultimately accelerate patient access.
Our solutions
Event schedule
Spotlight | 10:30am – 11:30am
Humans at the helm: Navigating increasing AI autonomy in HEOR and HTA
Speaker: Jaime Caro
Poster session 1 | 10:30am – 1:30pm
View list of posters and authors
Prescription trends and generic market share of heparinoid preparations in Japan from FY2014 to FY2024[c1.1]: A longitudinal claims database study
Dimitra Lambrelli et. al
Leveraging specialist ophthalmology EMR data to evaluate real-world effectiveness of anti-VEGF therapies for diabetic macular edema
Nick Boucher, Nitika Aggarwal, Mark Yates
Health state utilities associated with otoferlin-related hearing loss
Louis S. Matza, Timothy A. Howell, Nick C. Patel, Peter Quon, Paul Sommer, Ivette Cejas, Donald M. Goldberg, Jameel Muzaffar, Chad Ruffin
Health state utilities associated with treatment for transfusion-dependent ß-thalassemia in France
Louis Matza, Adeline Durand, Katie D. Stewart, Jennifer Drahos, Gabriela Vega-Hernandez
Changes in the number of pregnancy and lactation post-marketing requirements/commitments issued by the FDA after the release of the draft post approval pregnancy safety studies guidelines in 2019
Yassaman Vafai
Cost implications of declining MMR coverage in England: A two-cohort analysis of NHS burden and catch-up vaccination value
Kerry Winter
MLUMR: An R package for population-adjusted indirect comparisons using multilevel unanchored meta-regression
Ahmad Sofi-Mahmudi, Conor Chandler
Estimating the UK population eligible for late-line multiple myeloma therapies using an epidemiological model
Kang Kang, Shujun Li, Denise Zou
Understanding evidence and reimbursement pathways for oncology retreatment: A cross-country assessment of regulatory, guideline, and HTA perspectives
Anna D’Ausilio, Himani Jaiswal, Caroline Delaitre-Bonnin
Comparison of GPT-5 models for artificial intelligence (AI)-assisted data extraction from randomized clinical trials (RCTs) in systematic literature reviews (SLRs): Accuracy, reproducibility, and time-efficiency
Mariana Farraia, Aiswarya Shree, Archana Rajadhyax, Anuja Pandey, Sohan Nitin Deshpande, Carolina Casañas i Comabella
Mental health HEOR evidence generation and growth of real-world evidence amid increasing disease burden: An AI-assisted longitudinal analysis, 2014–2023
Corrina Mau, Weicheng Ye, Thitima Kongnakorn
Symposium | 12:15pm – 1:15pm
One JCA, many decisions: Building an evidence strategy for portability across Europe
Speakers: Caoimhe Rice, Martin Parkinson, Carla Dias Barbosa, Victoria Federico Paly
Poster session 2 | 4:00pm – 7:00pm
View list of posters and authors
Fit-for-purpose recruitment in decentralized observational studies: Innovations, use cases, and design considerations
Elizabeth Donahue, Alison Rushby, Christopher Morris, Neil R. Brett
An AI- enabled digital twin for simulating anti-VEGF treatment strategies in real-world nAMD care
Ashwin Rai, Ariel Berger
Content validity evaluation of selected patient-reported outcome measures for pain, fatigue, and physical functioning in adults, adolescents, and children living with Osteogenesis Imperfecta
Elizabeth Gibbons, Laura Kelly, Savita Bakhshi Anand, Stephanie Bascle, Joshua Maher, Tracy Hart, Cemre Robinson, Ethen Cheng, Ingunn Westerheim
A mapping gap in the new UK EQ-5D-5L era: Implications for health technology assessment
George Bungey et.al
Early economic and pathway impact of incorporating novel mass spectrometry-based testing into treatment response assessment for multiple myeloma
Gregory L. Price, Teofilo Borunda Duque
Assessing orphan medicines under the European union (EU) health technology assessment regulation (HTAR): Is current HTA guidance fit for purpose?
Andreas Freitag, Elena Aruffo, Hefin Thoma, Caroline von Wilamowitz-Moellendorff
PICO provenance evaluating AI traceability for EU joint clinical assessments
Hanna-Liisa Vilu, Victoria Molenkamp, Rhythm Arora
Workshop | 4:45pm – 5:15pm
Mixture cure models: Do they create more issues than they are trying to solve?
Speaker: Irina Proskorovsky
Research podium | 4:45pm – 5:45pm
Ready for prime time? Evaluating large language models for automated extraction of cost-effectiveness models from HTA submissions
Speaker: Simone Rivolo
Poster session 3 | 10:30am – 1:30pm
View list of posters and authors
Beyond expected outcomes: A framework to account risk aversion when eliciting patient preferences for treatment pathways in oncology
Hui Lu, Sebastian Heidenreich, Anup Das, Nicolas Krucien
A practical framework for including dietary data in real-world evidence studies: Lessons from inflammatory bowel disease and paediatric rare diseases
Neil Brett, Garthiga Manickam, Liz Donahue, John Sampalis, Susan Oliveria
Development of an integrated framework and AI-assisted platform for trustworthy regional healthcare data utilization in China
Zhen Luo, Hang Xu, Dimitra Lambrelli, Lu Ban
Adapting RWE methods to Japan: A practical framework for regulatory, ethical, and site-level implementation
Mika Kawaguchi, Tadashi Koga, Marina Yamamoto, Dimitra Lambrelli
Applying a framework to characterise the evolution of integrated scientific advice
Jennifer Boss, Emily Hearne, Marine Beugre-Guyot, Almudena Olid Gonzalez
The sensitivity analysis paradox in target trial emulation: An empirical taxonomy of bias mitigation and protocol design in 208 studies
Alban Fabre et.al
What drives positive NICE healthtech decisions? A review of economic evaluation evidence from recent appraisals
Vladislav Berdunov, Claire Spencer
From approval to access: Time to reimbursement decision for biosimilars in the EU-4
Alexandra Kumichel, Maria Dvorkina, Katherine Gibbs
Issue panel | 1:45pm – 2:45pm
Train the economist or hire the engineer? The future of expertise in AI-native HEOR
Speaker: Jaime Caro
Poster session 4 | 4:00pm – 7:00pm
View list of posters and authors
Should we collect patient preference insights in registries? Findings from the PPD CorEvitas Obesity Registry
Hui Lu, Kevin Patrick Marsh, Sebastian Heidenreich, Jennifer Whitty, Anup Das, Nicolas Krucien, Heather Chubb
Closing the language gap in HEOR reviews: Validating AI-assisted screening of Chinese-language evidence
Caroline von Wilamowitz-Moellendorff, Aiswarya Shree, Andreas Freitag, Caoimhe Rice, Mireia Raluy Callado, Jade Thurnham, Ziyi Li, Lu Ban
Feasibility of identifying HR+/HER2− metastatic breast cancer and CDK4/6 inhibitor-treated cohorts in a Japanese multicenter oncology EMR database
Motoki Kuzuya, Shigemi Matsumoto, Ayanori Fukushima, Dimitra Lambrelli, Tadashi Koga, Masafumi Okada, Manabu Muto
Beyond claims data: A legally governed integrated EHR-claims database for real-world evidence generation in Japan
Dimitra Lambrelli et.al
Environmental impact assessment for total knee replacement care pathway and subsequent prosthetic joint infection
Eva Fuchs, Tom Binstead, Caoimhe T Rice
A mathematical appraisal of the family and caregiving effects framework in modeling caregiver spillover effects
George Bungey et. Al
Real-world treatment patterns in chronic lymphocytic leukemia: A systematic review
Magdalena Monica, Monika Reczek, Pawel Kawalec, Katherine Gibbs
The best of both worlds? hybrid programmatic-ai workflows for HTA-grade evidence generation for time-to-event analysis interpretation and reporting
Simone Rivolo, Tereza Lanitis, George Bungey, Michalis Galanakis, Ivan Houisse, Jack Ishak
Using tokenization to overcome limitations of claims data to identify use of remote patient monitoring among patients with peritoneal dialysis
Firas M. Dabbous, Divya Shridharmurthy, Rhonda Shaw, Samuel Huse, Kathryn Evans, Vanessa Danielson, Ariel Berger
Workshop | 4:45pm – 5:15pm
Accounting for preference heterogeneity in stated choice data: From good-practice methods to decision-relevant interpretation
Speaker: Sebastian Heidenreich
Issue panel | 8:00am – 9:00am
How should evidence be assessed in rare diseases?
Speaker: Jaime Caro
Poster session 5 | 9:00am – 11:30am
View list of posters and authors
Real-world evidence (RWE) readiness for EU Joint Clinical Assessment: Gap analysis between current RWE studies and EU HTA expectations
Neil Brett, Garthiga Manickam, Deborah Tallarigo, Susan Oliveria, Jack Ishak, Roy Mootooswamy
Progression of metabolic dysfunction-associated steatohepatitis and economic burden: Use of real-world health record data in England to inform economic models
Jennifer A. Davidson, Hannah R. Brewer, Caoimhe Treise Rice, Sara J. Carvalho, Yestle Kim
Prevalence of potentially inappropriate prescribing (PIP) in older adults in 2025 in the United States: Can we do better in the digital age?
Kathryn Evans, Ade Agbemuko, Harmony Omeife, Ariel Berger
Estimating the fiscal impact of menopause symptoms in England and Wales: A public finance framework for the evaluation of menopause interventions
Kinga Marczell et. al
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