Are you ready to meet the new IEC 60601-1 Amendment 2 requirements?
Medical device standards are updated often. This can make it difficult for medical device manufacturers to keep up with the latest changes, impacting their quality systems and technical documentation, product development schedules, and time to market.
Join us on September 21 at 10 am EST to learn about the latest changes to IEC 60601-1.
Hosted by a certification expert, this one hour webinar will walk you through:
• Changes to process standards and how they affect IEC 60601-1 evaluations
• Major changes to ISO 14971:2019 from prior editions
• Usability Engineering process IEC 62366-1:2015 compliance
• Software development process IEC 62304:2006/62304:2006/Amd. 1:2015 compliance
• Major changes to the medical electrical equipment general standard
• Changes to alarms standard IEC 60601-1-8
Don't miss this opportunity to speak directly with a technical expert.
Register now.
Key Learning Objectives
- Changes to process standards and how they affect IEC 60601-1 evaluations
- Major changes to ISO 14971:2019 from prior editions
- Major changes to the medical electrical equipment general standard
- Software development process IEC 62304:2006/62304:2006/Amd. 1:2015 compliance
