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MHRA – Medical devices regulatory reform roadmap to implementation (from Catapult’s regulatory round-up for December 2024)

The MHRA published a revised roadmap towards the future regulatory framework for medical devices on 11th December 2024. This provides a further update on the intended timelines to implement the future medical device regulations. New guidance on post-market surveillance is expected to be published in June 2025, guidance on pre-market requirements is expected in 2026, and an in vitro diagnostic roadmap is expected to be published by September 2025.

Published on the 9th of January 2025. Read the entire Regulatory Round-up – December 2024.


OpenEdition vous propose de citer ce billet de la manière suivante :
adelage (12 février 2025). MHRA – Medical devices regulatory reform roadmap to implementation (from Catapult’s regulatory round-up for December 2024). ELSIBI. Consulté le 16 mars 2026 à l’adresse https://doi.org/10.58079/13axv


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