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Time: 9:00am EST

Duration: 60 minutes

Language: English

Cost: Free of charge

In order to ensure patient safety, constantly emerging technologies and product innovations require regulators and standard development organizations to permanently advance and adapt existing standards to the latest state of technology. A basic standard for all medical devices is the EMC (Electromagnetic Compatibility) standard 60601-1-2. This standard was published in its latest version, the 4th Edition, in 2014 (IEC, EN 2015) and is now a mandatory requirement for all medical device manufacturers.

Join CSA Group’s, Harald Buchwald, Technical Advisor – EMC, as he addresses and answers the following questions related to the 4^th Edition:

• What should be considered during product development?
• What are the differences to 60601-1-2 3rd Edition?
• Which products are mostly affected by the new standard?
• What happens to existing certified products?

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