#474: Behind the QMSR Audits: The Top 5 FDA C...

In this episode of the Global Medical Device Podcast, host Etienne Nichols continues his conversation with regulatory consultant Michael Drues, Ph.D., to examine the FDA's Center for Devices and Radiological Health (CDRH) guidance document priorities for fiscal year 2027. The dis ...  Show more

In this episode of the Global Medical Device Podcast, host Etienne Nichols and regulatory consultant Mike Drues dive deep into the world of FDA guidance documents. They unpack what these documents truly represent—the agency's current thinking rather than binding law—and explore h ...  Show more

Today's guest is Urvashi Tyagi, Advisor and Former CTO at ResMed. Urvashi joins us on today's podcast with Emerj Senior Matthew DeMello to discuss the unique challenges healthcare leaders face in driving software development efficiencies for medical devices and customer-facing ...

Our guest Ritu Agarwal, PhD, and Robert H. Smith Dean’s Chair of Information Systems and founding director of the school’s Center for Health Information and Decision Systems (CHIDS) discusses using digital technology, analytics, and AI to educate the next generation of health IT ...  Show more

Zack talks with legal tech expert Britt Lorish about the process of selecting and managing technology in large and small law firms. Listen in as they talk about typical pain points, common setups, and how process documentation is the first step you know you need to take but don’t ...  Show more

In this episode, Laura's off yelling at clouds, and the notable Jess Ivins steps in to talk about learning, education and how to keep growing as a UX person. Jess says smart and helpful things while Kate rambles on but does get in some good references to articles she did not writ ...  Show more