CiteMed

Conversations shaping the future of medtech.

Medtech is changing fast, and so is what it takes to show a device is safe and performs as intended. The Evidence Room is where the people doing that work come together to take a closer look at the facts, ask the sharp questions, and share what they’re learning along the way.

Each episode, CiteMed CEO Ethan Drower sits down with a guest from across clinical, regulatory and quality to talk through how clinical evidence is evolving under EU MDR, IVDR and FDA QMSR: what’s working, what isn’t, and where it’s heading next. From CERs and PMCF to literature reviews and Notified Body expectations, we get specific, so you leave with insights you can bring back to your team.