Skip to main content

Please note this is an extract of the original bulletin.

Notify the MHRA about a clinical investigation for a medical device

Page summary:
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.

Change made:
Added template for submitting Quarterly Summary Reports.

Medical devices: UK approved bodies

Page summary:
UK approved bodies listed under Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002).

Change made:
Updated page to include TUV SUD BABT Active Implantable Medical Devices Scope.

 

Tehelj