Regulating medical devices in the event of a no-deal Brexit
Posts published in “UK”
BSI certifies first product to the Medical Devices Regulation
Assistive technology: definition and safe use
Prep for Brexit: UK Seeks £25M Freight Service to Deliver Medicines, Devices
Contingency legislation covering regulation of medicines and medical devices in a no deal scenario – Human Medicines and Medical Devices (Amendment etc.) (EU exit) Regulations…
MHRA guidance updated to reflect the MDR – Clinical investigations of medical devices – Biological safety assessment
BSI – ISO 13485 and products with May 2020 deadline for MDR certification
Medicines and Healthcare Products Regulatory Agency Annual Report and Accounts 2018 to 2019
Dental radiographic X-ray imaging: dose to patients
MHRA launches consultation on how to best engage patients and the public