Please note this is an extract of the original bulletin.
Register medical devices to place on the market
Page summary:
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Change made:
Clarification concerning fees and actions required to change legislation of a registered device.
The Innovative Devices Access Pathway (IDAP)
Page summary:
The Innovative Devices Access Pathway (IDAP) program is designed to accelerate the development of cost-effective medical devices and their integration in to the UK market.
Change made:
Updated to add that the IDAP Pilot is closed for applications.
