MHRA ramps up assessment capacity for in-vitro diagnostic devices 30 Jan 2023

The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has extended the designation of UL International UK Ltd as an Approved Body. This means that the company can now assess almost all Part IV In-vitro Diagnostics Medical Devices and provide UKCA certification. This move aims to ensure that patients gain access to the medical products they need.