PQ 3920
3920. Deputy Pádraig O'Sullivan asked the Minister for Health the steps her Department has taken to give effect to Ireland's obligations under Regulation (EU) 2021/2282 on health technology assessment, including the obligation to give due consideration to Joint Clinical Assessment reports in national health technology assessments; the reason no guidance has been issued to marketing authorisation holders on how Joint Clinical Assessments will be considered in the reimbursement process (details supplied) ; whether she will direct that such guidance be published, setting out the process, timelines and the manner in which Joint Clinical Assessment reports will be factored into reimbursement recommendations by the National Centre for Pharmacoeconomics and the Health Service Executive; and if she will make a statement on the matter. [58155/26]
Introduced
28 July 2026
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28 July 2026
Summary
3920. Deputy Pádraig O'Sullivan asked the Minister for Health the steps her Department has taken to give effect to Ireland's obligations under Regulation (EU) 2021/2282 on health technology assessment, including the obligation to give due consideration to Joint Clinical Assessment reports in national health technology assessments; the reason no guidance has been issued to marketing authorisation holders on how Joint Clinical Assessments will be considered in the reimbursement process (details supplied) ; whether she will direct that such guidance be published, setting out the process, timelines and the manner in which Joint Clinical Assessment reports will be factored into reimbursement recommendations by the National Centre for Pharmacoeconomics and the Health Service Executive; and if she will make a statement on the matter. [58155/26]
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EU Regulations
EU Regulations
xml · EN · 28 July 2026
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- Official source: https://www.oireachtas.ie/en/debates/question/2026-07-28/3920/
- Open data entity: https://data.oireachtas.ie/ie/oireachtas/question/2026-07-28/pq_3920