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Human Factors/ Usability Studies following ISO 62366 , the FDA Guidance and the new FDA Draft Guidance

Human Factors/ Usability Studies following ISO 62366 , the FDA Guidance and the new FDA Draft Guidance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-based Design Control - The New Paradigm for Medical Device Design

Risk-based Design Control - The New Paradigm for Medical Device Design

Overview: Risk management overarches projects associated with a particular product family, giv..

Date : 17th February 2022

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

Duration : 1 Hour 10 Mins

Risk Based Design Control Requirements and Industry Best Practices for Medical Devices

Risk Based Design Control Requirements and Industry Best Practices for Medical Devices

Overview: Design flaws — not manufacturing errors — continue to be the leading cause of medica..

Date : April 29, 2025

Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time

Duration : 60 Mins

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