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Reimbursement strategy

Market Access Strategy for Medical Devices in Europe

Strategic recommendations on the topic of market access pathways for medical devices and IVD tests

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White Paper: Clinical evidence requirements for the “Orderly Introduction of Medical Technologies” process in Sweden

Get insights from MTRC White Papers to advance your understanding on the evidence requirements guiding the national adoption of medical technologies in Sweden

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Reimbursement summary for angioplasty of arteries of lower extremities

This post presents an extract from our reimbursement analysis for angioplasty of arteries lower extremities using plain and drug-coated balloons (DCBs) for peripheral artery disease in England, France and Germany. Plain balloon angioplasty is reimbursement via DRG solely and DCBs are reimbursement via combination of DRG and add-on reimbursement.
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February 2026 recommendations from the Swedish Medical Technologies Product Council

The national framework for the Orderly Introduction of Medical Technologies is a staged process that includes horizon scanning, selection of products for evaluation, the MTP Council’s decision to develop recommendations, health economic evaluation by the Dental and Pharmaceutical Benefits Agency (TLV), and the issuance of recommendations by the MTP Council to Swedish regions. In some cases, the MTP Council may issue temporary recommendations advising regions to refrain from introducing a technology until the evaluation is completed and final recommendations are issued.

On February 20, 2026, the MTP Council issued a favorable recommendation to regions regarding the use of magnetic resonance imaging-guided focused ultrasound (MRgFUS) for the treatment of patients with essential tremor:

  • Treatment with MRgFUS (Exablate Prime) should be offered to patients with severe essential tremor who have insufficient effect from pharmacological treatment and who are not candidates for deep brain stimulation (DBS).
  • National collaboration should be established to optimize the number of treatments performed per equipment unit and to ensure patients’ equal access to treatment.

On February 18, 2026, the MTP Council issued an interim recommendation advising regions to refrain from the broad implementation of blood tests for the diagnosis of Alzheimer’s disease and to limit their use to specialist healthcare settings and clinical studies until sufficient evidence is available for a comprehensive assessment and final recommendation.

The tests in question are performed directly from a blood sample, in which the analysis identifies biomarkers reflecting accumulations of disease-causing amyloid-beta in plaques and a hyperphosphorylated variant, p-tau, which accumulates inside nerve cells. Some tests also analyze combinations of different biomarkers.

See more details in Swedish here and here.

This news is just one of about 300 market access news collected by our team in the premium subscription service Market Access Monitor every week from more than 80 organizations. Access our paid service to stay on top of all developments specifically for your products in Europe (reimbursement news) and globally (HTA news). Access is organized as an online Database and email alert formats. Contact us to get a free, three-month, no-obligation trial.