Kendra Murphy

Kendra Murphy is a seasoned regulatory affairs professional with extensive experience in medical device and in vitro diagnostic kit development and registration. Currently serving as a Senior Manager in Regulatory Affairs at IQVIA since February 2019, Kendra previously held roles such as Regulatory Affairs Manager and Senior Regulatory Affairs Specialist at Novella Clinical. Kendra's expertise includes developing regulatory strategies, preparing complex submissions for clinical research and commercial distribution, and ensuring compliance with various regulatory bodies. With a comprehensive background that spans positions at Riverain Technologies, Mammotome, Aurora Health Care, inVentiv Clinical Solutions, and Kelly Scientific Resources, Kendra has demonstrated proficiency in managing regulatory documents, timelines, and compliance processes throughout the career.