TÜV Rheinland is educating customers on changes to medical device testing with adoption of IEC 60601-1 3rd Edition.
Manufacturers of electromedical devices will find substantial changes to the 3rd Edition of IEC 60601-1. Most notable is the requirement of additional risk analysis. It’s crucial to understand the changes in the Standard.
Starting your transition to IEC 60601-1 3rd Edition early allows for advanced planning for compliance of your medical device testing and can reduce risk associated with the new requirements.
For additional information on the agenda, click here.
To register via PO, please fill out the form to the right, or email us for additional information.