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 th...
Publication Details
- Journal
- Industrias Culturais (Universidade de Coimbra)
- Published
- 2025-02-12
- DOI
- https://doi.org/10.58079/13axv
- Primary Topic
- Health Systems, Economic Evaluations, Quality of Life
- Type
- article
- Field-Weighted Citation Impact
- 0.00