Adrienne Lenz

Adrienne Lenz is a Principal Medical Device Regulation Expert at Hyman, Phelps & McNamara, P.C., a position held since September 2017, following a role as Senior Medical Device Regulation Expert. Prior experience includes serving as a Senior Consultant in Quality Assurance and Regulatory Affairs at Emergo Group and as a member of Pathway Regulatory Consulting, LLC, where the focus was on assisting medical device manufacturers with market authorizations in multiple regions. Adrienne held various roles at GE Healthcare from July 2004 to July 2010, including Regulatory Affairs Director, managing global regulatory affairs for life support solutions, as well as positions in regulatory affairs and quality engineering. Earlier experience includes serving as a Regulatory Engineer at Smiths Medical from November 1997 to July 2004. Adrienne holds a Master of Science in Physiology from the Medical College of Wisconsin and a Bachelor of Science in Biomedical Engineering from the Milwaukee School of Engineering.