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European Parliament adopts extension to MDR transition period

European Parliament adopts extension to MDR transition period

Following the European Commission’s 6 January vote to extend the Medical Devices Regulation (MDR) and In Vitro Diagnostic Medical Devices Regulation (IVDR) transition period, the European Parliament (EP) adopted the proposal on 16 February 2023.

23 Feb 2023
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UK Government publishes response to MHRA fee consultation

UK Government publishes response to MHRA fee consultation

The Government has published its response to the consultation on proposals for changes to the Medicines and Healthcare products Regulatory Agency’s (MHRA) statutory fees.

13 Feb 2023
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MHRA announces new international recognition framework for MAs from 2024

MHRA announces new international recognition framework for MAs from 2024

The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has confirmed that the European Commission Decision Reliance Procedure (ECDRP) has been extended to 31 December 2023. After that a new international recognition framework will be instituted, from 1 January 2024.

9 Feb 2023
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