UK MHRA · May 11, 2026

MHRA invites views on proposed changes to medical device regulation

MHRA publishes new pre-market regulatory requirements for medical devices and in vitro diagnostic devices entering the GB market and invites stakeholder views.

Medium obligation Framework Medical Devices & IVD UK Medical devicesIn vitro diagnosticsCE marking

New pre-market regulatory requirements for medical devices and in vitro diagnostic devices entering the GB market have been published.

Read the official source ↗

Published by UK MHRA. HealthSignal links to the original document; the summary above is extracted from the source text.