Countries adopt different methods and processes to evaluate the benefits and costs of health technologies. It is important to identify and analyse the factors that influence the uptake and use of these methods and processes across countries. In this paper, we introduce a regulatory governance approach to the analysis of convergence, divergence and hybridity in HTA methods, discussing and critically analysing national processes for HTA in two major European Union (EU) Member States: England and Germany. We argue that any reasonably sophisticated account of national approaches to HTA must recognise that globalisation and the emergence of advanced industrial society involves the potential for widely varying processes, methods and evidential re...
This is an Accepted Manuscript of an article published by Taylor & Francis in Expert Review of Pharm...
In this article, we review the development of health technology assessment (HTA) in England and Wale...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...
© 2017 University of Durham and John Wiley & Sons, Ltd Countries adopt different methods and process...
The new regulatory governance perspective has introduced several insights to the study of health tec...
Independent regulatory agencies (IRAs) for Health Technology Assessment (HTA) are a key means by whi...
The evaluation of medicines and medical technologies – also called Health Technology Assessment (HTA...
Health technology assessment (HTA) agencies have spread throughout Europe in the past twenty years. ...
© 2014 Elsevier Ireland Ltd. The new regulatory governance perspective has introduced several insigh...
Decision-makers throughout Europe have a common goal of raising health standards in order to improve...
Objective: The Italian National Healthcare System (NHS) is one of the most decentralised systems sin...
OBJECTIVE: Improving synergy among regulation, health technology assessment (HTA) and clinical guide...
This document is the accepted manuscript version of the following article: Nicola Allen, Stuart R. W...
Introduction: In January 2018 the European Commission published a Proposal for a Regulation on Healt...
Health technology assessment (HTA) has assumed an increasing role in health systems in recent years,...
This is an Accepted Manuscript of an article published by Taylor & Francis in Expert Review of Pharm...
In this article, we review the development of health technology assessment (HTA) in England and Wale...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...
© 2017 University of Durham and John Wiley & Sons, Ltd Countries adopt different methods and process...
The new regulatory governance perspective has introduced several insights to the study of health tec...
Independent regulatory agencies (IRAs) for Health Technology Assessment (HTA) are a key means by whi...
The evaluation of medicines and medical technologies – also called Health Technology Assessment (HTA...
Health technology assessment (HTA) agencies have spread throughout Europe in the past twenty years. ...
© 2014 Elsevier Ireland Ltd. The new regulatory governance perspective has introduced several insigh...
Decision-makers throughout Europe have a common goal of raising health standards in order to improve...
Objective: The Italian National Healthcare System (NHS) is one of the most decentralised systems sin...
OBJECTIVE: Improving synergy among regulation, health technology assessment (HTA) and clinical guide...
This document is the accepted manuscript version of the following article: Nicola Allen, Stuart R. W...
Introduction: In January 2018 the European Commission published a Proposal for a Regulation on Healt...
Health technology assessment (HTA) has assumed an increasing role in health systems in recent years,...
This is an Accepted Manuscript of an article published by Taylor & Francis in Expert Review of Pharm...
In this article, we review the development of health technology assessment (HTA) in England and Wale...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...