Webinar Search Results: 4	Topic: Not Specified	Category: All	Speaker: Edwin Waldbusser

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AI/ML Medical Device Regulation Following the new L...

AI/ML Medical Device Regulation Following the new Law and the 2025 FDA Guidance

AI/ ML will revolutionize medicine by making diagnosis and treatment more accessible and more effective.

Edwin Waldbusser

July 7, 2025
60 Minutes
US$149.00
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Medical Device Software Validation Meeting FDA Regulati...

Medical Device Software Validation Meeting FDA Regulations

This course will teach how to conduct a software validation program for medical devices containing software that will satisfy FDA requirements and produce a safe product.

Edwin Waldbusser

July 10, 2025
60 Minutes
US$149.00
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FDA Regulation of Artificial Intelligence/ Machine ...

FDA Regulation of Artificial Intelligence/ Machine Learning

AI/ ML will revolutionize medicine by making diagnosis and treatment more accessible and more effective.

Edwin Waldbusser

July 17, 2025
60 Minutes
US$149.00
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Human Factors/ Usability Studies following ISO62366...

Human Factors/ Usability Studies following ISO62366, the FDA Guidance, and the new FDA Draft Guidance

Human Factors/ Usability is the analysis of how people interact with medical devices. The process of conducting rigorous human factors studies throughout the design process, integrating it with the device risk analysis and design process, and validating the effectiveness of the studies will be explained.

Edwin Waldbusser

July 24, 2025
60 Minutes
US$149.00
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