Faster, Fairer, Broader: What NICE’s 2025–26 Annual Report Means for Market Access
Author: Ben Barron-Millar, Senior Consultant, Value Communication The National Institute for Health and Care Excellence (NICE) has published its Annual […]
Author: Ben Barron-Millar, Senior Consultant, Value Communication The National Institute for Health and Care Excellence (NICE) has published its Annual […]
Author: Ben Barron-Millar, Senior Consultant, Value Communication A summary of NICE’s disease-specific reference case extension for managing overweight and obesity
At HTAi 2026 in Istanbul, one message came through clearly: delivering high-quality health technology assessment (HTA) is no longer the
The EU HTA Regulation (EU) 2021/2282 was designed to transform clinical assessment in Europe through Joint Clinical Assessments (JCAs). But
Strategic Implications for Pharma & Biotech from ASCO 2026 Author: Univ.-Prof. Dr. Matthias P. Schönermark, Chief Strategy Officer Every
Authors: Prof. Dr. Matthias Schonermark, Chief Strategy Officer & Sebastian Vinzens, Senior Medical Writer The first EU JCA should not
Authors: Ben Hendry, Director, Global Business Development & Ruth Howells, Country Manager, UK & Ireland At ISPOR US 2026 in Philadelphia,
Author: Wim Neckebroek, Director, Regulatory Affairs The Belgian Federal Agency for Medicines and Health Products (FAMHP) has introduced new guidance
Author: Florian Stieglitz, Consultant, Market Access Germany’s draft contribution rate stabilization law for the statutory health insurance system (GKV-Beitragssatzstabilisierungsgesetz) has
Author: Lukas Schoppmeyer, Senior Consultant, Market Access Since 2019, following the adoption of the German Act for greater safety in the provision of medicinal products (GSAV), Section 35a