Background: To ensure rapid access to new potentially beneficial health technologies, obtain best value for money, and ensure affordability, healthcare payers are adopting a range of innovative reimbursement approaches that may be called Managed Entry Agreements (MEAs). Methods: The Health Technology Assessment International (HTAi) Policy Forum sought to identify why MEAs might be used, issues associated with implementation and develop principles for their use. A 2-day deliberative workshop discussed key papers, members' experiences, and collectively addressed four policy questions that resulted in this study. Results: MEAs are used to give access to new technologies where traditional reimbursement is deemed inappropriate. Three different f...
This systematic study aims at analyzing the differences between the approach of the European healthc...
In 2010, the Australian Government introduced the managed entry scheme (MES) to improve patient acce...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...
The reimbursement of expensive, innovative therapies poses a challenge to healthcare systems. This s...
: Managed entry agreements (MEA) represent one of the main topics of discussion between the European...
Background: Managed entry agreements (MEAs) continue to emerge in health technology assessment (HTA)...
Background: Market access stakeholders consider the adoption of Managed Entry Agreements (MEAs), how...
Objectives: Australia relies on managed entry agreements (MEAs) for many medicines added to the nati...
Performance-based managed entry agreements (PB-MEAs) might allow patient access to new medicines, bu...
This chapter provides an overview on Managed Entry Agreements (MEA). Managed Entry Agreements are co...
This chapter provides an overview on Managed Entry Agreements (MEA). Managed Entry Agreements are co...
Background: Despite the increased utilisation of Managed Entry Agreements (MEAs), empirical studies ...
BACKGROUND: Managed Entry Agreements (MEAs) are increasingly used to address uncertainties arising i...
Managed entry agreements (MEAs)—a type of formal institutional arrangement between pharmaceutical co...
Purpose: Centrally authorised medicinal products (CAMPs) in the European Union may offer added thera...
This systematic study aims at analyzing the differences between the approach of the European healthc...
In 2010, the Australian Government introduced the managed entry scheme (MES) to improve patient acce...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...
The reimbursement of expensive, innovative therapies poses a challenge to healthcare systems. This s...
: Managed entry agreements (MEA) represent one of the main topics of discussion between the European...
Background: Managed entry agreements (MEAs) continue to emerge in health technology assessment (HTA)...
Background: Market access stakeholders consider the adoption of Managed Entry Agreements (MEAs), how...
Objectives: Australia relies on managed entry agreements (MEAs) for many medicines added to the nati...
Performance-based managed entry agreements (PB-MEAs) might allow patient access to new medicines, bu...
This chapter provides an overview on Managed Entry Agreements (MEA). Managed Entry Agreements are co...
This chapter provides an overview on Managed Entry Agreements (MEA). Managed Entry Agreements are co...
Background: Despite the increased utilisation of Managed Entry Agreements (MEAs), empirical studies ...
BACKGROUND: Managed Entry Agreements (MEAs) are increasingly used to address uncertainties arising i...
Managed entry agreements (MEAs)—a type of formal institutional arrangement between pharmaceutical co...
Purpose: Centrally authorised medicinal products (CAMPs) in the European Union may offer added thera...
This systematic study aims at analyzing the differences between the approach of the European healthc...
In 2010, the Australian Government introduced the managed entry scheme (MES) to improve patient acce...
Much criticism has been directed at the licencing requirements for medical devices (MDs) as they oft...