PQ 991
991. Deputy Colm Burke asked the Minister for Health the person within the HSE who decides if a product is experimental in respect of the treatment abroad scheme; the criteria that this decision maker uses to decide such and the definitions applied to experimental treatments; if the relevant decision makers have the expertise to review drugs for complex conditions; if the existing reimbursement list is referred to in making reimbursement decisions or whether European Medicines Agency approval is deemed to be the overriding proof of clinical safety; and if he will make a statement on the matter. [37831/22]
Introduced
12 July 2022
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12 July 2022
Summary
991. Deputy Colm Burke asked the Minister for Health the person within the HSE who decides if a product is experimental in respect of the treatment abroad scheme; the criteria that this decision maker uses to decide such and the definitions applied to experimental treatments; if the relevant decision makers have the expertise to review drugs for complex conditions; if the existing reimbursement list is referred to in making reimbursement decisions or whether European Medicines Agency approval is deemed to be the overriding proof of clinical safety; and if he will make a statement on the matter. [37831/22]
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Healthcare Policy
Healthcare Policy
xml · EN · 12 July 2022
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- Official source: https://www.oireachtas.ie/en/debates/question/2022-07-12/991/
- Open data entity: https://data.oireachtas.ie/ie/oireachtas/question/2022-07-12/pq_991