Background: Managed entry agreements (MEAs) continue to emerge in health technology assessment (HTA)-based decision-making, to address evidentiary uncertainties arising therein. Evidence on the HTA criteria that influence MEAs' uptake remains scarce. This study explores the HTA criteria that determine (i) if an HTA funding decision will be listed with conditions (LWC) other than a MEA, or with a MEA as a condition (LWCMEA), and ii) the MEA type implemented (i.e., financial, outcomes based, or combination). Methods: HTA reports of all oncology medicines approved since 2009 in Australia, England, Scotland, and Sweden were searched to capture the clinical/economic evidence uncertainties raised in the decision-making process, the Social Value J...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...
Background Health technology assessment (HTA) has become an important policy tool for its ability to...
The use of health technology assessment (HTA) to inform policy-making is established in most develop...
BACKGROUND: Managed Entry Agreements (MEAs) are increasingly used to address uncertainties arising i...
Background: Despite the increased utilisation of Managed Entry Agreements (MEAs), empirical studies ...
Background Recent changes to the regulatory landscape of pharmaceuticals may sometimes require reim...
Recent changes to the regulatory landscape of pharmaceuticals may sometimes require reimbursement au...
Context. Positive health technology assessment (HTA) outcomes can have important implications for eq...
Background: To ensure rapid access to new potentially beneficial health technologies, obtain best va...
Background: Criticisms have emerged that cancer medicines offer modest benefits at increasingly high...
Objectives Health Technology Assessment (HTA) agencies produce recommendations that guide public fun...
Purpose: Centrally authorised medicinal products (CAMPs) in the European Union may offer added thera...
Objectives: Advanced therapy medicinal products (ATMPs) are highly innovative therapies. Their costs...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...
Background Health technology assessment (HTA) has become an important policy tool for its ability to...
The use of health technology assessment (HTA) to inform policy-making is established in most develop...
BACKGROUND: Managed Entry Agreements (MEAs) are increasingly used to address uncertainties arising i...
Background: Despite the increased utilisation of Managed Entry Agreements (MEAs), empirical studies ...
Background Recent changes to the regulatory landscape of pharmaceuticals may sometimes require reim...
Recent changes to the regulatory landscape of pharmaceuticals may sometimes require reimbursement au...
Context. Positive health technology assessment (HTA) outcomes can have important implications for eq...
Background: To ensure rapid access to new potentially beneficial health technologies, obtain best va...
Background: Criticisms have emerged that cancer medicines offer modest benefits at increasingly high...
Objectives Health Technology Assessment (HTA) agencies produce recommendations that guide public fun...
Purpose: Centrally authorised medicinal products (CAMPs) in the European Union may offer added thera...
Objectives: Advanced therapy medicinal products (ATMPs) are highly innovative therapies. Their costs...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...
Background Health technology assessment (HTA) has become an important policy tool for its ability to...
The use of health technology assessment (HTA) to inform policy-making is established in most develop...