MedTech Safety
Bio
Dr. Keith Morel is Scientific Lead of the Medical Device Business Unit, VP of Regulatory Compliance & Principal Consultant at Qserve Group, one of the largest European-based medical device consulting companies.
He has worked in the medical device industry since year 2000. Prior to joining Qserve, he was Senior Director for Regulatory Compliance at Accuray (a radiation oncology device manufacturer).
Keith was also a Senior Project Manager for DEKRA-Certification for 9 years. During his time at DEKRA he was a Quality System, and MDD lead auditor, as well as a design dossier reviewer. He performed more than 100 audits and 200 Design Dossie, Technical File, and Change reviews.
Before DEKRA, he worked in R&D in various roles as Engineer, Manager and Director, for several technologies including IVUS-catheters and super-oxidized water products. He holds both a First-Class degree and a Ph.D. in Physics from Imperial College of Science, Technology, and Medicine, in London.
In his spare time, Dr. Morel is an adjunct associate professor at the University of Southern California in the Regulatory Sciences program, teaching EU regulations, statistical process-control and risk-management. Please welcome Dr. Keith Morel.