Principal Regulatory Consultant
DLRC
Richard Bassett is a medical device quality and regulatory professional, with a comprehensive background encompassing the utilisation, research, and manufacturing of medical devices and in vitro diagnostics (IVDs). Currently serving as a Principal Regulatory Consultant at DLRC, a renowned regulatory affairs consultancy with a team of over 80 highly qualified regulatory professionals, Richard operates from the UK office, contributing to DLRC's success in strategically located offices across the UK, Germany, and the US.
Bringing to the table over 14 years of extensive experience within the medical device industry, Richard has held roles including quality management, regulatory compliance, and clinical strategy development. His expertise extends to effective supplier engagement and guiding product development. Richard's professional journey has traversed roles with a legal manufacturer, consultancy positions, and contributions to a Notified Body.
Richard holds a master's degree in molecular biology, complemented by a second master's degree in medical law, which specifically focused on UK and EU Medical Device Regulations. His dedication to sharing and imparting his knowledge is evident through his five year tenure as a lecturer on medical device regulatory affairs at Cambridge University, where he has made valuable contributions to the BioEnterprise MSc course.
As a Principal Regulatory Consultant at DLRC, Richard continues to bring his wealth of knowledge and hands-on experience to navigate the complex landscape of medical device regulations, contributing to DLRC's reputation as an award-winning consultancy.
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Wednesday, May 8, 2024
14:00 – 15:00 CEST