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News and blog posts

07
Apr 2022

Recommendations about add-on reimbursement for medical devices in France in February 2022

The French National Authority for Health (HAS) released new recommendations about add-on reimbursement of medical devices and medical aids from the meetings of the National Commission for Evaluation of Medical Devices and Health Technologies (CNEDiMTS) in February 2022. More than 25 recommendations were published in relation to the registration, modification of registration conditions, and renewal of registration of devices in the List of reimbursable products and services (LPPR). Opinions concern cardiovascular and peripheral vascular, orthopedic, neurovascular, and neuromodulation devices, as well as breast implants and medical aids. Except for this, CNEDiMTS published two negative opinions concerning transitional coverage of devices.
06
Apr 2022

Assessment of surgical procedures for obesity treatment released in Norway

On March 18, 2022, the Norwegian National Institute of Public Health released an HTA report on the evaluation of surgical procedures for obesity treatment. The authors concluded that it is uncertain whether there is any difference in the risk of early mortality and the effect on weight status between different types of surgical procedures for the treatment of obesity.
05
Apr 2022

Med Tech-related technology assessments and clinical guidelines from NICE in February 2022

In February 2022, the National Institute for Health and Care Excellence (NICE) published two new Interventional Procedure Guidance (stereotactic radiosurgery for trigeminal neuralgia, and microwave ablation for primary or metastatic cancer in the lung), two new Diagnostic Guidance (EarlyCDT Lung for assessing the risk of lung cancer in solid lung nodules, PredictSURE IBD and IBDX to guide treatment of Crohn's disease), and four new Medtech Innovation Briefings (Insides System for managing intestinal failure, d-Nav insulin management app for type 2 diabetes, GaitSmart for personalized exercise rehabilitation, AposHealth for knee osteoarthritis)
04
Apr 2022

The standard for telemonitoring of patients with implantable cardiac devices published in France

On March 17, 2022, the French National Authority for Health (HAS) published a standard for telemonitoring of patients with implantable cardiac devices (implantable defibrillators and pacemakers). In January 2022, the HAS also published standards for medical telemonitoring of four chronic pathologies (chronic respiratory failure, chronic heart failure, chronic renal failure, and diabetes). All these standards must be met by technologies in order to be reimbursed by the new reimbursement framework for telemonitoring, which is expected to enter into force in July 2022.
01
Apr 2022

Research demand signaling for the National Stroke Programme in England

On March 03, 2022, NHS England and NHS Improvement published a research demand signaling document for the National Stroke Programme. This document highlights the priority areas for research to inform national policy and support the NHS Long Term Plan targets. One of the high-priority areas is the technology for diagnosis, including artificial Intelligence solutions, innovative triage tools, technologies for the early and accurate diagnosis/detection of stroke.
31
Mar 2022

Rapid HTAs of two medical devices released in Tuscany

The HTA body of the Tuscany Regional Healthcare issues two types of documents: HTA forms and motivational forms. With regional decree 4229 of March 11, 2022, Tuscany Regional Healthcare has published assessments of two medical devices in the cardiovascular and ENT fields of care.
30
Mar 2022

Applications for the 2023/24 High Cost Device List are open in England

In March 2022, NHS England opened a call for applications to the High Cost Device List (HCDL) changes for the 2023/24 National Tariff Payment System. The completed application form should be submitted via email by May 31, 2022. HCDL items are then either included in a fixed payment or paid in addition to the price of the related service.
28
Mar 2022

2022/23 MedTech Funding Mandate policy published in England

In March 2022, NHS England and NHS Improvement published the MedTech Funding Mandate (MTFM) policy for 2022/23, which will come into force on April 01, 2022. The MTFM launched in 2021 to support NICE-approved and cost-saving devices, diagnostics, and digital products. Commissioners must fund technologies included in MTFM.
25
Mar 2022

Three projects awarded under the 2022 "Subsidy scheme for promising care" in the Netherlands

On March 4, 2022, the Dutch Healthcare Institute (Zorginstituut Nederland, ZIN) announced three projects which received a subsidy under the "Subsidy scheme for promising care" in 2022 for research of a new minimally invasive endoscopy-guided surgery in patients with spontaneous cerebral hemorrhage, oral immunotherapy in children to cure a food allergy and cutting the diaphragm band in chronic abdominal complaints.
24
Mar 2022

Rapid HTAs of five medical devices released in Tuscany

The HTA body of the Tuscany Regional Healthcare issues two types of documents: HTA forms and motivational forms. With a regional decree 2472 of February 10, 2022, Tuscany Regional Healthcare has published assessments of five medical devices of various therapeutic areas, such as cardiovascular and peripheral vascular areas.
23
Mar 2022

MTP Council updated recommendations on gene expression analysis for decision-making on the adjuvant breast cancer treatment

In late January 2022, Swedish Medical Technologies Product (MTP) Council issued an updated version of recommendations regarding gene expression analysis for decision-making on the adjuvant breast cancer treatment, initially published in November 2021. The recommendation to the regions remains the same. The changes were only concerned with the clarification of some facts.