As the Director of QA/RA, Ian is responsible for the overall running and effectiveness of Team Consulting’s Quality Management System and leading the QA/RA team. He is also responsible for collaborating with other internal business partners to identify ways in which clients can be served in meeting their existing and future regulatory objectives.
“Medical device regulations are undergoing transformational change, particularly in the EU/EEA and in the UK. The introduction of new regulations such as the MDR and IVDR and the advent of UKCA marking due to Brexit are presenting a significant challenge to medical device companies in understanding their regulatory obligations.”
“I strongly believe that Team can be a true partner to clients in helping to structure a successful regulatory strategy, and can in the process, cement Team as a partner of choice for medical device development now and in the future.”
Ian has worked within the medical device industry for over 20 years and has extensive experience in both blue-chip corporate, start-up, and SME organisations across a range of medical devices and IVDs. Ian coordinated the transition of a medical devices manufacturer to MDR compliance for a class III insulin pump and helped a start-up in Cambridge to secure UKCA marking for a novel cholesterol test utilising a smartphone.
