Associate Director Regulatory Affairs
Abbott
Jenny Chan, MS, RAC, PMP, is an Associate Director of Regulatory Affairs in the Medical Devices division of Abbott, with over 16 years of experience in active implantable medical device regulatory affairs. She is an accomplished regulatory affairs professional with a focus in the cardiovascular and neuromodulation medical device space, and has been instrumental in securing numerous product approvals throughout her career. Jenny has a Bachelor's in Biomedical Engineering and a Master's in Regulatory Science from the University of Southern California. She began her regulatory career at Boston Scientific Neurmodulation working on SCS technologies for chronic pain prior to joining Thoratec, later St. Jude Medical, and now Abbott, where she worked on LVAD technologies for chronic heart failure and currently MEMS technologies for heart failure remote monitoring. Jenny has a deep understanding of the complexities of the regulatory landscape and is known for her ability to navigate complex regulatory challenges with ease. Her extensive knowledge of the medical device industry and strong relationships with regulatory bodies make her a sought-after expert in her field. At RAPS Convergence 2023, Jenny will share her insights and experiences with navigating medical device EU MDR challenges with notified bodies to obtain approvals. Attendees can expect to gain valuable knowledge and practical tips that they can apply to their own regulatory affairs work.
Disclosure information not submitted.
Solutions Circle: Medical Device EU MDR Lessons Learned with Two Different Notified Bodies
Wednesday, October 4, 2023
12:05 PM – 12:35 PM EDT