MHRA - Medical devices regulatory reform roadmap to implementation (from Catapult's regulatory round-up for December 2024)
Year: 2025
Type: other
Abstract: 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...
Source: Hypotheses (OpenEdition)
DOI: 10.58079/13axv
Author: Adelage
Language: English
Topic: Healthcare Regulation
Subfield: Health Information Management
Field: Health Professions
Domain: Health Sciences
Open Access status: green
OpenAlex ID: W6954834807
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