Are you harnessing the full power of IEC 62366-1 to enhance user safety and improve device usability in your medical device development?
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
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:
- Overview of IEC 62366-1
- Exploring Types of Use Errors
- Enhancing Safety with IEC 62366-1
- Collaboration between Quality Assurance & Human Factors
- Navigating the Regulatory Landscape
- Mastering Formative and Summative Evaluations
- Our Top Tips for User-Centered Design
The webinar is 100% virtual and 100% free. You won’t wanna miss it!
