Programpunkter

The European project Label2Enable (2022–2024) has tested how ISO/TS 82304-2 can be used to assess the quality and trustworthiness of health apps. The standard was tested as a common framework for transparency regarding security, quality, and information content.The results show that ISO/TS 82304-2 has potential as a common European reference, in line with the requirements of the European Health Data Space (EHDS) for trust, interoperability, and quality and trustworthiness. The work has continued, and the standard is currently applied to varying degrees in several European countries.

In this session, Tomaž Gornik will build on the Postmodern EHR concept and explore how it is now maturing through two powerful forces: artificial intelligence and national-scale platform deployments. What began as an architectural vision is increasingly becoming the operating model for regions, countries, and large healthcare systems seeking both innovation and long-term resilience.

Oral

Symposia/Panel

Oral

Workshop

AI is everywhere in healthcare software, but when is it actually safe? This session explains what separates regulated medical-grade AI from uncontrolled tools, how manufacturers manage LLM unpredictability, and what questions buyers should ask any vendor claiming clinical AI capabilities.

Oral

Oral

Oral

Oral

The talk will explain the full journey of creating a Software as a Medical Device from concept to certification. It will outline the key stages including defining intended use, design and usability engineering, regulated software development, clinical evaluation strategies and the CE marking process. The session will also highlight differences between class I and higher class SaMD products which require more rigorous controls and notified body involvement. The presentation will share realistic minimum timelines and cost ranges based on completed European projects to help companies plan their investment and avoid common pitfalls.

Healthcare systems face rising costs and growing pressure to improve results, yet decisions are still often based on activities and assumptions rather than measured value across the full care pathway. This session shows how outcomes, patient experience, and total cost can be measured together at pathway level for defined conditions, making trade-offs visible and supporting informed clinical and management decisions grounded in real results. By treating care as a long-term investment and using reproducible models over time, organizations can improve outcomes, manage resources responsibly, and create value for patients and society.

Oral

Oral

This session presents Region Stockholm's ongoing work on the HL7 FHIR standard.

Get a glimpse of tomorrow’s healthtech breakthroughs at the Healthtech Startup Pitch Event, where 6 promising startups presents their solutions.

Healthcare regions and laboratories are facing rising data complexity and increasing demands for interoperability and precision medicine. Traditional Laboratory Information Management Solutions (LIMS) are not built for this environment. This session introduces how the Nordic Data Model provides a modern data architecture that connects laboratory data with clinical context and analytics, enabling a shift from volume-oriented operations to value driven services. Participants will see how this approach supports smarter testing, stronger decision making and scalable regional infrastructures.