UK Parliament / Open data

Medicines and Medical Devices Bill

Moved by

Baroness Wheeler

119: After Clause 38, insert the following new Clause—

“Northern Ireland and regulatory divergence

(1) The Secretary of State must work together with the appropriate authority in Northern Ireland to minimise the potential for and mitigate against regulatory divergence in relation to human medicines, veterinary medicines and medical devices.

(2) Where the Secretary of State has identified areas of regulatory divergence in relation to human medicines, veterinary medicines and medical devices between Northern Ireland and the rest of the UK, the Secretary of State must lay a report before both Houses of Parliament setting out how the divergence will impact—

(a) the UK; and

(b) Northern Ireland.

(3) The report must set out the steps the appropriate authorities have taken to mitigate against such divergence.”

Member’s explanatory statement

This Clause would require the Secretary of State to work with the appropriate authority in Northern Ireland to minimise the potential for regulatory divergence relating to medicines and devices, and report any areas of regulatory divergence to Parliament, including the impact they will have, and report on actions to mitigate against adverse consequences arising from divergence.

About this proceeding contribution

Reference

807 cc684-5GC 

Session

2019-21

Chamber / Committee

House of Lords Grand Committee
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