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A DECADE OF HEALTH TECHNOLOGY ASSESSMENT IN POLAND

Published online by Cambridge University Press:  19 July 2017

Iga Lipska
Affiliation:
Department of Science, Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht [email protected]
Neil McAuslane
Affiliation:
Center for Innovation in Regulatory Science
Hubert Leufkens
Affiliation:
Department of Science, Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht University
Anke Hövels
Affiliation:
Department of Science, Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht University

Abstract

Objectives: The objective of this study is to illustrate and provide a better understanding of the role of health technology assessment (HTA) processes in decision making for drug reimbursement in Poland and how this approach could be considered by other countries of limited resources.

Methods: We analyzed the evolution of the HTA system and processes in Poland over the past decade and current developments based on publicly available information.

Results: The role of HTA in drug-reimbursement process in Poland has increased substantially over the recent decade, starting in 2005 with the formation the Agency for Health Technology Assessment and Tariff System (AOTMiT). The key success factors in this development were effective capacity building based on the use of international expertise, the implementation of transparent criteria into the drug reimbursement processes, and the selective approach to the adoption of innovative medicines based on the cost-effectiveness threshold among other criteria.

Conclusions: While Poland is regarded as a leader in Central and Eastern Europe, there is room for improvement, especially with regard to the quality of HTA processes and the consistency of HTA guidelines with reimbursement law. In the “pragmatic” HTA model use by AOTMiT, the pharmaceutical company is responsible for the preparation of a reimbursement dossier of good quality in line with HTA guidelines while the assessment team in AOTMiT is responsible for critical review of that dossier. Adoption of this model may be considered by other countries with limited resources to balance differing priorities and ensure transparent and objective access to medicines for patients who need them.

Type
Theme Submissions
Copyright
Copyright © Cambridge University Press 2017 

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References

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