Anders Orn

Anders Orn has conducted successful human factors and usability research for more than 50 medical devices, including surgical instruments, point-of-care devices, diagnostics, combination products, Class III devices, home-use devices, OTC products, and more. He is especially valued for helping companies understand and navigate regulatory human factors, guiding companies of all sizes through submissions to United States Food and Drug Administration (FDA) and European Union Medical Device Regulation (MDR).