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Market access for medical technologies in Sweden

A brief overview of key market access pathways and challenges for medical devices, in-vitro diagnostic tests in Sweden

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Key topics

There are three key themes describing market access for medical technologies in Sweden: 

  • Reimbursement: payment mechanism via the DRG-adjusted budget system
  • Funding: recommendations in the national “Orderly Introduction of Medical Technologies” framework
  • Health technology assessment: obtaining recommendations from the national and regional HTA bodies
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Reimbursement

Hospital care is predominantly funded via a global budget adjusted for activity based on DRGs. 

Sweden shares the DRG system (NordDRG) with several other countries, including Finland and Norway. However, all inter-regional care is reimbursed on a case-by-case basis via the DRG system. Therefore, the role of DRG is higher for procedures, which are concentrated only in several hospitals across the country and which provide care for patients from other Swedish regions. 

DRGs are determined by the combination of a procedure code (KVÅ) and a diagnosis code (ICD-10). KVÅ nomenclature is maintained by the National Board of Health and Welfare and released annually. The Swedish version of the NordDRG system is approved annually, and the base rate is determined at the national level.

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Funding

Sweden has no nationally defined list of health benefits which are guaranteed to the Swedish population. Decisions on which treatment methods to use and which new technologies to introduce are made by the hospitals.

Swedish regions have a system to collaborate on the introduction of medical technologies and to enable equal access, cost-effective and efficient use of medical technologies in the country (“Orderly Introduction of Medical Technologies” framework). In this framework, technologies are evaluated on the national level, and recommendations for the adoption of novel technologies are provided to payers (Regions) and healthcare providers. 

Two organizations play a key role in the framework: 

  • MTP Council initiates the HTAs and makes final recommendations for adoption
  • The Dental and Pharmaceutical Benefits Agency (TLV) performs horizon scanning activities to identify relevant topics for evaluation and full health technology assessments (with a heavy focus on the health economic evaluation) of the procedures selected for evaluation by the MTP Council. 
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Health technology assessment

HTA is performed on the national level (as part of the “Orderly Introduction of Medical Technologies” or as stand-alone evaluations) or on the regional level (which can inform regional/local decision-making).

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Specifics for IVD tests

There is no specific reimbursement framework for in-vitro diagnostic tests. IVD tests are funded using a global budget principle as part of the laboratory funding.

MTRC has experience with more than 206 projects in Sweden

News and insights

Ongoing assessments by the HTA Center of Västra Götaland Region in Sweden as of June 2026

As of June 2026, the HTA Center of the Västra Götaland Region in Sweden is conducting six health technology assessments across areas such as gynecology, orthopedics, neurology, and in-vitro diagnostics.

Changes in responsibilities for managing coding classifications in Sweden

From June 1, 2026, certain responsibilities will be transferred from the National Board of Health and Welfare (Socialstyrelsen) to the Swedish eHealth Agency (E-hälsomyndigheten). These include responsibility for managing classifications, including procedure coding (KVA) and diagnosis coding (ICD-10-SE). Responsibility for the diagnosis-related groups (DRG) system will remain with the National Board of Health and Welfare.

February 2026 recommendations from the Swedish Medical Technologies Product Council

In February 2026, the Swedish Medical Technologies Product (MTP) Council issued two recommendations to Swedish regions within the national framework for the Orderly Introduction of Medical Technologies. The first recommendation concerns MR-guided focused ultrasound (Exablate Prime), which is recommended for patients with severe essential tremor. The second is an interim recommendation advising regions to refrain from introducing diagnostic blood tests for Alzheimer’s disease until the MTP Council has conducted a comprehensive assessment and issued final recommendations.

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