Implications of IEC 60601 3rd edition Webinar
TÜV SÜD Product Service is hosting a complimentary webinar on the 3rd. edition of 60601 on 30th November 2011, 2pm
Overview of Presentation
The latest in a series of webinars discussing the changes in the electrical safety testing requirements for electrical medical devices.
With the end of the transition period of the 3rd edition of the IEC 60601-1 standard fast approaching (June 2012), manufacturers and designers of active medical devices will already be part way through or at the end of the transition to the 3rd edition. Some will however only just be starting.
No matter at what stage you are at meeting the requirements of the 3rd edition, this webinar will provide confirmation that the work was done adequately, highlight any issues still to be completed, or it may even provide an interesting idea of how to implement the 3rd edition more efficiently for your next product.
Who should attend:
- All test engineers
- Design engineers
- Regulatory professionals and quality professionals involved or planning to be involved in electrical medical devices
Benefits of attending:
- To understand the implications of the 3rd edition on your product designs and/or redesigns
- To hear about some issues that exist within the 3rd edition of 60601
CLICK HERE TO REGISTER YOUR INTEREST
