Webinar Oct. 6: Applying IEC 62304 Principles to Electrical and Mechanical in Medical Device Design

Velentium is pleased to partner with Greenlight Guru to present a free live webinar, “Extending IEC 62304’s Software Lifecycle Principles to Electrical and Mechanical in Medical Device Design,” with Greenlight Guru’s Etienne Nichols and Velentium’s Satyajit Ketkar, on Thursday, October 6th at 1:00pm EST.

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Velentium is pleased to partner with Greenlight Guru to present a free live webinar, “Extending IEC 62304’s Software Lifecycle Principles to Electrical and Mechanical in Medical Device Design,” with Greenlight Guru’s Etienne Nichols and Velentium’s Satyajit Ketkar, on Thursday, October 6th at 1:00pm EST.

IEC 62304 started out as a functional safety standard, but since its release in 2006, it has become the standard for process life cycle for software. This includes safety classification and has a relationship to other medical device standards like ISO 13485, ISO 14971, IEC 60601 and IEC 63266. It provides principles of what needs to be done as part of medical device software for technical and management roles and aspects.

In this free, in-depth webinar, Satyajit ‘Sat' Ketkar, Velentium’s Director of Systems Engineering, will explain how these principles can and should be applied to all functions of a medical device, specifically electrical and mechanical life cycles, to provide consistency for process elements like Requirements, Risk Analysis, Failure Mode Analysis Architecture, Design, Implementation, Test, Traceability as well as consistency in language, i.e Items, Units.

Participants will learn how to apply these principles to the entire medical device life cycle, leading to more efficient design, development and manufacturing. Register for this free webinar, which will provide consistent guidance to all engineers and a better mechanism of planning for the project managers.

Learn more and register at https://www.greenlight.guru/webinar/iec-62304-principles-electrical-mechanical-device-design-partner.

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