Nieuwsbrief
HTA Quarterly Spring 2026
In this edition, we discuss the risks of relying on immature data for survival projections in oncology and the importance of selecting robust models to guide HTA decisions. We also explore key challenges and developments in HTA within the UK and Germany, including the impact of limited clinical evidence on NICE appraisals, with strategies to improve submission outcomes, and recent updates to Germany’s AMNOG dossier requirements, highlighting the evolution to trend-based estimates to better align benefit assessments with statutory health insurance patient populations.
Heard on the street
“The HTACG estimates that it will initiate around 50 joint clinical assessments (JCAs) of medicines… and for the first time, JCAs of selected high-risk medical devices.”
— EU’s Member State Coordination Group on Health Technology Assessment (HTACG) outlining key strategic priorities for 2026
Source: Health Technology Assessment – 2026 Work Programme adopted
Source: Health Technology Assessment – 2026 Work Programme adopted
HTA by the numbers
200%
The new HTACG target of 50 JCAs in 2026 is twice the target number of JCAs for 2025.
Sources:
Health Technology Assessment – 2026 Work Programme adopted
New EU rules for health technology assessments become effective | European Medicines Agency (EMA)
Sources:
Health Technology Assessment – 2026 Work Programme adopted
New EU rules for health technology assessments become effective | European Medicines Agency (EMA)
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Ons ervaren team van waarde-experts creëert op basis van bewijsmateriaal, beleidsinzichten en marktinformatie effectieve strategieën voor toegang tot wereldwijde markten. We maken u wegwijs in de complexe wereld van de gezondheidszorg in verschillende delen van de wereld. Neem contact op om te ontdekken hoe we uw doelen kunnen ondersteunen.
