FREE LIVE WEBINAR
May 9, 2024 | 1-2:30 pm ET / 10-11:30 am PT

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

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 where medical device development experts from CLEIO will dive deep into IEC 62366-1, guiding you through the intricacies of the regulatory framework and risk management around the standard.

Whether you’re looking to refine your current processes or integrate new methodologies, this session will provide you with the knowledge and tools you need to apply this critical standard effectively to make your devices safer and more user-friendly.

Specifically, this webinar will cover:

• Overview of IEC 62366-1: Explore key elements of the standard and its practical implementation in enhancing medical device usability.
• Types of Use Errors: Understand the three main types of use errors identified in medical device usage
• Enhancing User Safety: Learn about the safety benefits that IEC 62366-1 brings to users and its importance in medical device design
• Collaboration between QA & HF: Discover how Quality Assurance (QA) and Human Factors (HF) integrate to strengthen medical device development
• Navigating the Regulatory Landscape: Get an overview of the regulatory framework and the essentials of risk management
• Mastering Usability Engineering Validation: Gain key insights into formative and summative evaluations and their critical roles in the design process
• Top Tips for User-Centered Design: Acquire practical strategies to optimize your development process with a focus on User-Centered Design