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Cost-effective reimbursement analysis for medical technologies in Europe

Procedure coding, payment mechanism, reimbursement tariffs, policy, and HTA considerations in 20 EU countries

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White Paper: Evidence Requirements for Interventional Procedures Program at NICE in the United Kingdom

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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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Med Tech-related technology assessments from NICE in October 2025

Health Technology Evaluations (HTE) using the Early Value Assessment (EVA) approach are the new type of NICE guidance to provide rapid conditional recommendations on promising health technologies that have the potential to address unmet national needs. NICE evaluates the available evidence to determine if earlier patient and system access in the NHS is appropriate while further evidence is generated. 

In October 2025, NICE published one new EVA on Artificial Intelligence (AI) technologies to aid opportunistic detection of vertebral fragility fractures and concluded that five technologies can be used in the NHS during the evidence-generation period as options to aid the opportunistic detection of vertebral fragility fractures: BriefCase-Triage, CINA-VCF Quantix, HealthOST, HealthVCF, and IB Lab FLAMINGO. These technologies can only be used according to their indications, as outlined in the instructions for use, and with consideration of the risk groups as recommended in NICE’s guideline on osteoporosis: assessing the risk of fragility fracture. More research is needed on Annalise Enterprise CXR/Annalise Container CXR, BoneView, and TechCare Spine. 

The National Institute for Health and Care Excellence (NICE) develops Interventional Procedures Guidance (IPG) for most novel interventional procedures entering the English market. The program focuses solely on clinical evidence. Recommendations may vary from "for research only" to "for use with standard arrangements for clinical governance, consent, and audit." Recommendations are not binding, although they are followed by providers and commissioners. 

In October 2025, NICE released two new IPGs with the following recommendations: 

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.