Med-Tech Innovation January 9, 2024

The Medicines and Healthcare products Regulatory Agency (MHRA) has set out new plans for the development of new regulations for medical devices in the UK.

The government says the new regulations will put patient safety first and help to ensure that patients continue to have access without delay to the devices they need, whilst enhancing the UK’s position as a world-leading environment for medical technology innovators.

This new ‘roadmap’ for new regulations from the MHRA aims to enhance the UK’s ability to benefit from rapidly advancing medical technology, offering new opportunities for patients and healthcare.

The MHRA’s roadmap sets out a route to deliver enabling regulation via a series of new Statutory...

Today's Sponsors

LEK
ZeOmega

Today's Sponsor

LEK

 
Topics: Govt Agencies, Medical Devices, Regulations
Don’t Erode Medical Device Trust with Right to Repair
Neuralink, Passive BCIs And The Future Of Neuroadaptive Technology
AdvaMed itemizes AI imperatives for ‘the entire healthcare ecosystem’
Inaugural Meeting for FDA's Digital Health Advisory Committee to Focus on GenAI-enabled Medical Devices
Blood vessel-like coating could make medical devices safer for patients

Share This Article