We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » UK Regulator Clarifies When Standalone Software is a Device
UK Regulator Clarifies When Standalone Software is a Device
The UK’s Medicines and Healthcare products Regulatory Agency issued guidance late last month clarifying when standalone software qualifies as a medical device from a regulatory standpoint.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor