Written answers

Friday, 7 September 2018

Department of Health

Medicinal Products Reimbursement

Photo of John BrassilJohn Brassil (Kerry, Fianna Fail)
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592. To ask the Minister for Health the reason there is no specific budget for orphan drugs as committed to in the drugs and rare disease policy; and if he will make a statement on the matter. [35512/18]

Photo of Simon HarrisSimon Harris (Wicklow, Fine Gael)
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In Ireland the majority of patients access medicines through the publicly funded Community Drug Schemes.

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 including clinical benefit and cost effectiveness and does not include a separate ruleset or budget provision for orphan drugs.

In line with the 2013 Act, if a company would like a medicine to be reimbursed by the HSE pursuant to the Community Drugs scheme, the company must first submit an application to the HSE to have the new medicine added to the Reimbursement List.

As outlined in the IPHA agreement, 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), to either add the medicine to the reimbursement list or agree to reimburse it as a hospital medicine, or refuse to reimburse the medicine.

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.

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