Post by Michael Hottner
Medical Device Regulatory Affairs Expert | US 510(k) & EU MDR Specialist | ISO 10993 Biological Safety Specialist | Bridging Product Development & Regulatory Strategy | 15+ Years MedTech | StraightForward Consulting
Final interview video from my recent MedtecLIVE visit 🎤 This time, I had the pleasure of speaking with Dr. Marcus Jenke from Use-Ing 🤝 about a topic that is often underestimated during product development: Usability Engineering and Human Factors. In the medical device world, safety is not only determined by technology and performance. It is equally important that users can operate a device safely and as intended. A well-executed usability process helps identify use-related risks early, improve the user experience, and ultimately contribute to safer products for patients and healthcare professionals 👨⚕️👩⚕️ Many thanks to Marcus for sharing his insights and practical experience 👏 This concludes my little trade fair interview series. A big thank you to all interview partners for taking the time to share their expertise and perspectives with the community 🙏 #MedicalDevices #UsabilityEngineering #HumanFactors #IEC62366 #MedTech #RegulatoryAffairs #ProductDevelopment
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