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Human Factors/ Usability Studies following ISO 62366 , the FDA Guidance and the new FDA Draft Guidance

Human Factors/ Usability Studies following ISO 62366 , the FDA Guidance and the new FDA Draft Guidance

Overview: Human Factors/Usability studies are essential in ensuring that medical devices are ..

Date : 25th June 2024

Time : This Event is Over and the Recorded Content is Available

Duration : 75 Mins

Risk Management for ML medical devices following BS/AAMI 34971:2023 and ISO 14971

Risk Management for ML medical devices following BS/AAMI 34971:2023 and ISO 14971

Overview: FDA has always prioritized the risk management of medical devices, adhering to its ..

Date : 27th February 2024

Time : This Event is Over and the Recorded Content is Available

Duration : 60 Mins

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