This forum is a collection of stories and content from our team that talks about what’s happening in the medical device industry, the changing landscape, and how companies and talents are positioning themselves.

Steve C de Baca, Chair of Patient Safety and Quality Officer at Philips, speaks on how a singular letter changed the trajectory of his career (for the better!), as well as on ‘analysis paralysis’, where companies become so driven by fear that they don’t want to take risks in fixing broken things, and so much more!

Olga van Grol-Lawlor, the Manager of Global Regulatory Intelligence & Advocacy at Boston Scientific, talks on the importance of embracing a positive and proactive mindset within the workplace, how she ha overcame imposter syndrome, as well as how she went from working in equine science to the field of regulatory!

Suzie Halliday, the Vice President of Regulatory at BSI, shares her insights into the future of AI within the regulatory world, her career at a Notified Body, and much more!

Tom Melvin, Associate Professor of Medical Device Regulatory Affairs at Trinity College Dublin, discusses how knowing patients on a personal, human-level is key, as well as how specific regulations will be needed to be carved out specifically for AI.

Mario Wijker, Senior Vice President of RA/QA at Bio-Rad, talks on the process of steps one’s company should take to foster a culture of quality.