Dáil Éireann Debate, Thursday - 15 November 2018
112. Deputy Maureen O'Sullivan asked the Minister for Health if he is satisfied with the timeframe in place for access to new medicines while tentative steps must be taken before a medicine is approved; and his views on whether the extent of the timeframe is problematic for persons suffering with certain conditions. [47471/18]
View answerThe HSE has statutory responsibility for medicine pricing and reimbursement decisions, in accordance with the Health (Pricing and Supply of Medical Goods) Act 2013. The Act specifies the criteria for decisions on the reimbursement of medicines. As Minister for Health, I do not have any statutory power or function in relation to the reimbursement of medicines.
In line with the 2013 Act, if a company would like a medicine to be reimbursed by the HSE, it must first submit an application to have the new medicine added to the reimbursement list.
As outlined in the 2016 Framework Agreement with the Irish Pharmaceutical Healthcare Association (IPHA), and in line with the 2013 Act, the HSE will decide, within 180 days of receiving the application (or a longer period if further information is sought from the company), whether to add the medicine to the reimbursement list, agree to reimburse it as a hospital medicine, or refuse to reimburse it.
HSE decisions on which medicines are reimbursed by the taxpayer are made on objective, scientific and economic grounds, on the advice of the National Centre for Pharmacoeconomics (NCPE).
The NCPE conducts health technology assessments (HTAs) for the HSE and makes recommendations on reimbursement to assist HSE decisions. The NCPE uses a decision framework to systematically assess whether a drug is cost-effective as a health intervention.
The HSE strives to reach a decision in as timely a manner as possible. However, because of the significant monies involved, it must ensure that the best price is achieved, as these commitments are often multi-million euro investments on an on-going basis. This can lead to a protracted deliberation process.
I am keen to engage with industry and to explore ways in which new medicines might be more easily introduced in Ireland. However, any innovative approaches that may be tabled must be compatible with the statutory provisions which are in place and must also recognise the context of finite Exchequer resources.
I am aware that at the recent bi-annual meeting between my Department and the Irish Healthcare Pharmaceutical Association that this proposed dialogue was discussed. It is envisioned that this will take the form of a structured platform of engagement, building a stronger partnership between the State and industry to create better patient access to new treatments.
