Principal Regulatory Consultant
NAMSA
Kevin’s has over 20 years’ experience in the medical devices field, working in industry and for multiple Notified Bodies and moved to NAMSA in January 2021 in a Regulatory Consultancy role. An electronic engineer by training, Kevin spent time in the telecoms and nuclear industries. Upon joining the medical device industry Kevin worked for companies such as Elekta and Gambro and went on to serve at two medical device notified bodies, leaving SGS United Kingdom in December 2020, after having held many roles, most recently as the Notified Body Global Medical Devices Certification Manager.
Kevin joined the medical device consulting team at NAMSA in January 2021. His work at NAMSA has focused on complex submissions primarily for active devices, including: development of regulatory and clinical strategies and MDR transition strategies; technical documentation compilations; MDR QMS transition consultations; the new United Kingdom UKCA regulatory process; and regulatory due diligence.
Disclosure information not submitted.
Monday, September 12, 2022
9:45 AM – 11:00 AM MST