Tuesday, 9 October 2018

Ceisteanna (329)

Charlie McConalogue

Ceist:

329. Deputy Charlie McConalogue asked the Minister for Health if access to new treatments for MS patients (details supplied) will be introduced; and if he will make a statement on the matter. [41051/18]

Amharc ar fhreagra

Freagraí scríofa (Ceist ar Health)

The 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 through the community drugs schemes, it must first submit an application to the HSE 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 have indicated a willingness to meet with MS Ireland and a mutually convenient date has been agreed provisionally in the coming weeks.