Events

Don’t Miss Our Webinar on IEC 62366-1 with Greenlight Guru

Are you harnessing the full power of IEC 62366-1 to enhance user safety and improve device usability in your medical device development?

In an industry where the margin for error is minimal and user safety is paramount, understanding and implementing IEC 62366-1 can be the game-changer your projects need.

Join us for an insightful webinar with two experts from CLEIO: Maude Leclerc-De Guire (Human Factor Specialist) and Jean-Yves Pairet (Quality Assurance Director). They will dive deep into IEC 62366-1, guiding you through the complexities of the regulatory framework and risk management around the standard.

The Essentials of IEC 62366-1: Elevating User Safety in Medical Devices

Live Session
May 9 | 1:00 pm UTC−4

This session is designed to equip you with a deep understanding of the IEC 62366-1 standard, emphasizing how it is leveraged by medical device development experts to significantly enhance user safety and improve device usability. Dive into the definition of the standard, understand the types of use errors, and explore the critical roles of Quality Assurance and Human Factors in the development process.

Discover practical strategies to implement IEC 62366-1 effectively within your projects, ensuring compliance and optimizing user-centered design.

Whether you’re looking to refine your current processes or seeking new methodologies to apply to make your devices safer and user friendly, this webinar will provide you with the knowledge and tools needed to elevate your practice and drive safe innovation in medical device development.

Specifically, this webinar will cover:

The webinar is 100% virtual and 100% free. You won’t wanna miss it!

Author & collaborators

Written by
Caroline

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