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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: Evidence requirements for Med Tech Early Value Assessment at NICE in the United Kingdom

Get insights from MTRC White Papers to explore the analysis of five HTAs of digital and diagnostic technologies and strategic recommendations for evidence generation strategy in the UK

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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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Funding call for evidence generation on NICE early use technologies in England

On April 8, 2026, the National Institute for Health and Care Research (NIHR) opened a new call under its Invention for Innovation (i4i) Product Development Awards (PDA), focused on supporting technologies recommended by NICE for early use in the NHS, conditional on evidence generation.

The scope of the call is focused on producing real world evidence, or other relevant evidence, required by NICE early use assessment (in line with NICE early use recommendations and evidence generation plans) to achieve a full NICE evaluation, generation of real world evidence required by commissioners to encourage increased uptake and use of technologies within the NHS and social care settings, and capturing learnings for generalizable guidance for innovators.

Eligible products are those already approved for early use in the NHS through NICE early use guidance (early value assessment). Technologies that have received negative or research-only recommendations from NICE are not eligible for this funding opportunity.

Applications must be submitted by consortia that include an analytical partner acting as the lead applicant, a technology partner (the product provider), and at least one NHS site or service adopting the technology. Projects can run for up to three years and are expected to generate the required evidence within the timeframe specified by NICE.

Funding is flexible, with no fixed upper or lower limit, provided costs are well justified and demonstrate value for money. SMEs and NHS organizations may receive up to 100% of the requested funding, with no requirement for matched funding from commercial partners. Higher Education Institutions are entitled to up to 80% of the full economic costs. Large enterprises are expected to provide in-kind contributions.

The application process is structured in two stages:

  • To apply for the first stage, an outline application should be submitted by May 27, 2026. 
  • Successful applicants will then be invited to submit a full application from August 5 to September 23, 2026.
  • Notification of the final funding decision is expected from December 2026 at the earliest.

To support applicants, NIHR will host a webinar on April 15, 2026, providing an overview of the PDA scheme and this specific funding opportunity, along with details on scope, requirements, and the application process, followed by a live Q&A session.

See the full details 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.