Don't get bogged down making the transition to IEC
60601-1 3rd edition


Medical device manufacturers will find substantial changes to the 3rd Edition of IEC 60601-1. Most notable is the requirement of additional risk analysis. The added responsibility of risk mitigation on the manufacturer has implications for getting new products to market, and can be overwhelming to medical device designers and original equipment manufacturers (OEMs). Failure to implement this new requirement can result in delaying your product to market and in lost revenue. It’s crucial to understand the changes in the Standard and how those changes affect you as a medical device manufacturer. This webinar will examine the changes to IEC 60601-1 3rd Edition and the reason for the changes. Manufacturers and designers will learn about the impact to your business, as well as the actions, steps and deadlines to ensure a smooth transition to the 3rd Edition.

Date: November 10, 2011
Time: 1PM CT | 2PM ET
Webcast Duration: 60 minutes


Dale Hallerberg

Dale Hallerberg
Technical Manager, Medical Product Testing
TÜV Rheinland of North America

For more information about our speaker, please click here


Rich Nass

Rich Nass
Director of Content
UBM Canon

For more information about our moderator, please click here


Sponsored by:   TÜV Rheinland