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Realizing Safe, Intuitive User Interfaces: Key Considerations for Regulated Medical Devices
Regulatory focus on Human Factors and Usability Engineering provides an opportunity for device OEMs to improve the usability and safety of their products/devices. Despite the common view that regulation is only a burden, human factors analysis (HFA) can yield tangible benefits beyond the realization of safe, intuitive user interfaces that meet today’s regulatory standards. By adopting the best practices from this guidance, device OEMS can improve their development processes, avoid costly rework and delays, and ultimately deliver value to their customers. 

Jan 17, 2023 11:00 AM in Eastern Time (US and Canada)

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