Following recent market developments, we have made the strategic business decision to exit from these services. We are also withdrawing our application to become a Netherlands-based EU Notified Body for these services and furthermore, will not be applying to become a Notified Body for Medical Devices Regulation (MDR) or In-Vitro Diagnostic Devices Regulation (IVDR).
We will, however, continue to provide ISO 13485 third party certification and medical devices-related training to clients both in the UK and worldwide.
We are working closely with the UK Medicines and Healthcare Products Regulatory Agency (MHRA) to help customers which hold certification for these Directives with LRQA transfer to an alternative service provider.