How the HTAR will contribute to a value‐based decision‐making for medicinal products across the EU
The European Union Health Technology Regulation 2021/2282 (HTAR) introduces joint assessment of health technologies (including medicinal products and medical devices) across EU Member States. It was signed into law in 2021 and came into full force in January 2025.
Roisin Adams, Michal Stanak
wiley +1 more source
The EMU: forerunners and durability [PDF]
The first article examines the history and theory of monetary unions to ask what factors will foster a stable European Monetary Union. It concludes that a decentralized arrangement of national central banks may undermine the EMU’s durability.European ...
Robert F. Graboyes
core
Beyond one-size-fits-all: leveraging mixed-methods qualitative analysis of local stakeholders to tailor validated prehospital care solutions in the Cameroonian cultural context. [PDF]
OConnor K +12 more
europepmc +1 more source
Abstract Despite regulatory progress being made in the past two decades, off‐label drug use in paediatrics remains pervasive, with prevalence estimated between 3% and 97% of prescriptions across different clinical settings. Off‐label use—defined as prescribing outside the conditions described in the Summary of Product Characteristics (SmPC)—is often ...
Tjitske M. van der Zanden +3 more
wiley +1 more source
Fiscal Reform and Monetary Union in West Africa [PDF]
The paper explores the interaction between the proposed monetary union for ECOWAS and structural reforms of fiscal policy. The effects depend to a large extent on the degree of similarity of member countries.
Hefeker, Carsten
core
Leaving the health workforce during the COVID-19 pandemic: A cross-sectional study among Filipino healthcare workers. [PDF]
Tiu CJS +4 more
europepmc +1 more source
Zuranolone: A case study in (regulatory) rush to judgement?
Abstract Sage, in collaboration with Biogen, submitted a new drug approval for zuranolone for postpartum depression (PPD) and major depressive disorder (MDD) in December 2022. In August 2023, the US Food and Drug Administration granted approval for PPD but denied approval for MDD.
Lisa Cosgrove +4 more
wiley +1 more source
Inclusiveness of social participation for health reform: findings from a realist review. [PDF]
Mishra S +8 more
europepmc +1 more source
Abstract Aim To identify safety concerns reported by coroners following fentanyl patch‐related deaths in England, Wales and Northern Ireland, and determine differences in coronial reporting. Methods A systematic case series linking the National Programme on Substance Use Mortality (NPSUM) and the Preventable Deaths Tracker (PDT) (https ...
Eman Mshari +2 more
wiley +1 more source
Socio-economic Conditions & Determinants of Income: A Tale of Informal Workers of Urban Odisha, India. [PDF]
Barik S, Mishra NK, Saxena M.
europepmc +1 more source

