The MHRA is implementing the Medical Devices (Amendment) (Great Britain) Regulations 2025 to reform how medical devices are classified, registered, and regulated in Great Britain following Brexit. The framework covers device scope, classification systems, economic operator responsibilities, data protection, and UDI requirements. Recent activity includes consultation on fetal dopplers and alignment with the Medicines and Medical Devices Act 2021.
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom
In response to: Consultation on the future regulation of medical devices in the United Kingdom