Pharmaceutical companies have a good understanding of the needs and requirements of regulatory bodies, but the evidence expectations of health technology assessment (HTA) and coverage/payer bodies are less well understood and addressed. This paper seeks to improve this understanding by providing an overview of the expectations of HTA and coverage/payer bodies, explaining how and why these differ from those of regulators, and describing the extent and limitations of work on harmonization. The article goes on to describe ways in which HTA and coverage/payer bodies ’ expectations can be addressed, and to encourage industry to interact with HTA and coverage/payer bodies to increase mutual understanding and hence promote more efficient developme...
Background: Health technology assessment (HTA) has increased in importance in supporting payer decis...
Health technology assessment (HTA) was introduced in Australia for the reimbursement of pharmaceutic...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...
This is the final version of the article. Available from the publisher via the DOI in this record.Th...
The use of health technology assessment (HTA) to inform policy-making is established in most develop...
This article discusses the development of Heath Technology Assessment methods and HTA institutions, ...
This article intends to give an overview about developments in European Regulatory and Health Techno...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...
Health Technology Assessment (HTA) has emerged as an important tool to support healthcare decision-m...
To achieve the goal of improving the health of the population, all health systems need to take deci...
Countries in the Balkan region use pharmaco-economic data for decisions about the inclusion of new p...
The article presents the description of structural, organizational and methodological issues of heal...
The need to optimize drug development and facilitate faster access for patients has ignited discussi...
Objectives: National health technology assessments (HTAs) across Europe show differences in evidenti...
The systematic use of evidence to inform healthcare decisions, particularly health technology assess...
Background: Health technology assessment (HTA) has increased in importance in supporting payer decis...
Health technology assessment (HTA) was introduced in Australia for the reimbursement of pharmaceutic...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...
This is the final version of the article. Available from the publisher via the DOI in this record.Th...
The use of health technology assessment (HTA) to inform policy-making is established in most develop...
This article discusses the development of Heath Technology Assessment methods and HTA institutions, ...
This article intends to give an overview about developments in European Regulatory and Health Techno...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...
Health Technology Assessment (HTA) has emerged as an important tool to support healthcare decision-m...
To achieve the goal of improving the health of the population, all health systems need to take deci...
Countries in the Balkan region use pharmaco-economic data for decisions about the inclusion of new p...
The article presents the description of structural, organizational and methodological issues of heal...
The need to optimize drug development and facilitate faster access for patients has ignited discussi...
Objectives: National health technology assessments (HTAs) across Europe show differences in evidenti...
The systematic use of evidence to inform healthcare decisions, particularly health technology assess...
Background: Health technology assessment (HTA) has increased in importance in supporting payer decis...
Health technology assessment (HTA) was introduced in Australia for the reimbursement of pharmaceutic...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...