Duncan McPherson, MBBS FRCA

Clinical Director of Devices
MHRA

Dr Duncan McPherson, MBBS FRCA, is Clinical Director of Devices at Medicines and Healthcare products Regulatory Agency, UK. He is a registered specialist in anesthesiology and a Fellow of the Royal College of Anaesthetists.

He was a consultant anaesthetist at Queen Alexandra Hospital, Portsmouth until 2018 where he was head of anaesthesia patient safety. He worked for the National Patient Safety Agency as a clinical adviser and has undertaken research on epidemiological methods for describing avoidable harm and on patient safety incident reporting systems.

Currently he is leading the Devices Clinical Team at MHRA. Devices Division at MHRA is the national competent authority for regulating medical devices and in vitro diagnostic devices in the UK. They work to generate continuous improvement in the safety, effectiveness and usability of medical devices.

Presentation(s):

• Broad Stakeholder Panel Debate on Status of Implementation of the EU Medical Device Regulations MDR and IVDR

  Monday, September 23
  10:30 AM – 12:00 PM

• Interactions with Health Authorities

  Monday, September 23
  1:00 PM – 1:55 PM

• Managing the Requirements of the EU Medical Device Regulation General Safety and Performance Requirement 10.4.1.

  Monday, September 23
  2:05 PM – 3:00 PM

• Interactions with Health Authorities

  Tuesday, September 24
  2:05 PM – 3:00 PM