I really enjoy the field of medical device regulatory, and teaching is one way to spread the joy and engage others.
Part Time Assistant Professor
I really enjoy the field of medical device regulatory, and teaching is one way to spread the joy and engage others. There is always something to learn, and it is a field where one can continue to learn.
In the field of medical device regulatory, one is exposed to all the new developments with medical devices. This is evolving very quickly and thus makes the regulatory requirements interesting, as the technology is often novel and moving very quickly. There is so much rapidly occurring: AI, sensors and data collection, et al. In addition, a second area that I am fascinated by is the concept of regulatory reliance. This is the idea of leveraging regulatory authorizations in one country to facilitate review in the next country.
I hope to engage and excite based on my enthusiasm and interest. I hope students gain my joy and enthusiasm for the field and see how much interesting data there is available on different medical devices.
I wish I had more time for hobbies, though with two reasonably active boys, I spend a fair amount of time chauffeuring and butlering. I really enjoy manual driving and try to insist that this is part of my daily driving. I view fitnessing as a means for enjoying food, and I don’t believe I’ve ever met a salad I disliked.
Evangeline Loh Zielinski is a Regulatory Affairs Professional with two decades of experience assisting medical device manufacturers with global regulatory compliance. She has a distinguished record of leveraging her regulatory expertise with her personal and communication skills to achieve regulatory collaboration and success. She is an expert in European market access and compliance, global regulatory requirements, global post-marketing surveillance and vigilance, and global regulatory strategy. She leverages her biomedical education (Ph.D.) and intellectual curiosity, RAPS Regulatory Affairs Certification (RAC in US and EU), and regulatory experience to tackle regulatory projects.