This question has been answered by the relevant Government Department.
To ask Her Majesty's Government what process will be followed for Northern Ireland in circumstances where the Medicines and Healthcare products Regulatory Agency approves a licence for a medicine but such approval has not been given by the European Medicines Agency.
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† Item that is new or altered.
[I] Indicates that the member concerned has a relevant registered interest.
* Item is an oral question.
Numbers starting HL are unique identifiers for written questions, Bills or papers.
Member's Registered Interests
There are no interests to show.