How to Test to IEC 60601-1, 3rd Edition
This webinar provides up-to-date, detailed information about ANSI/AAMI ES60601-1:2005, Medical electrical equipment—Part 1: General requirements for basic safety and essential performance and its requirements for manufacturers of medical electrical equipment—both in the U.S. and overseas. Deadlines for compliance with 60601-1 are rapidly approaching—manufacturers face a June 2012 deadline for products sold in the EU and Canada and a June 2013 deadline in the US. Watch this webinar to learn more about the changes in the 3rd edition: new definitions and expansion of risk management processes in Amendment 1, information on safety testing options and gap testing, and a manufacturer’s view on compliance.
| WHO SHOULD PURCHASE |
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| This webinar is intended for design engineers, scientists, quality assurance professionals, regulatory professionals, test laboratories, and any other individuals responsible for the development of medical electrical equipment. |
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| QUESTIONS? | |
For questions about ordering the CD, please contact AAMI publications at 1-877-249-8226 or 240-646-7031. |
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PROGRAM OBJECTIVES
- Overview of the first amendment’s risk management changes
- Safety testing options explained
- IEC 60601-1:2005, 3rd edition gap testing
- A manufacturer’s view on compliance
SPEAKERS
- Joe Murnane, BSEE, Underwriters Laboratory, Inc.
- Frank O'Brien, BSEE, MS, O'Brien Compliance Management, LLC
- Brodie Pedersen, Nonin Medical
WEBINAR CD
- Includes pdf of handout materials and webinar recording on CD.
- $295 for webinar registrants
- $395 for non-registrants
- domestic and international shipping rates apply
WAYS TO PURCHASE
- Online - Click here to order online.
- Phone - 1-877-249-8226 or 240-646-7031 to order with a credit card.
- Fax - Select and download the order form and fax to 240-396-5781.
- Mail - Select and download the order form and mail with payment to:
AAMI Webinar CD
How to Test to IEC 60601-1, 3rd Edition
PO Box 0211
Annapolis Junction, MD 20701-0211