Gino Kenny (Dublin Mid West, People Before Profit Alliance) | Oireachtas source

A key recommendation of the national rare disease plan of the previous Government was to establish a rare disease technology review group. I understand there is a chair but no members. The Minister understands and is cognisant of the serious situation in this country whereby citizens cannot get certain drugs because of a very flawed process. This is a life or death situation for citizens and the Minister is aware of this. Will he comment on when this will be set up?

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