Webinar: Designing for regulatory compliance – how safety and EMC updates to the IEC 60601 series will affect your products
In this one-hour webinar Intertek’s experts on safety and EMC of electrical medical equipment will explain what the standard updates mean for construction and testing as well as give practical tips on how to make regulatory testing as efficient as possible
During the fall of 2020, the main family of standards for safety and EMC of electrical medical devices – IEC 60601 – underwent major updates. These updates affect compliance testing of these products, and therefore how future products should be designed to be compliant.
In this one-hour webinar (including time for questions), Intertek’s experts on safety and EMC of electrical medical equipment will explain what the standard updates mean for construction and testing as well as give practical tips on how to make regulatory testing as efficient as possible.
Who should attend?
Do you work in product development or compliance for electrical medical equipment? Then this webinar is relevant for you.
Jenny Larsson Falk is Technical Leader for medical equipment testing for Sweden and Regional Lead Engineer Medical for laboratory and measurement equipment for EMEA at Intertek. She chairs SEK TK66 – “Safety of measuring, control and laboratory equipment” and is a member of SEK TK62AD – “Electrical equipment in medical practice”, IEC SC62A WG14, MT28 and MT30, and of the IECEE CTL Expert Task Force 3.
Hasnain Hassanali is Senior EMC Engineer at Intertek and has worked with EMC and radio testing of medical devices for over 20 years. Since 2004, he is an EMC expert member of MT23 and TK62A and has lectured on IEC60601-1-2 around the world since 2008.