際際滷shows by User: IntertekNorthAmerica / http://www.slideshare.net/images/logo.gif 際際滷shows by User: IntertekNorthAmerica / Thu, 31 Oct 2013 11:33:36 GMT 際際滷Share feed for 際際滷shows by User: IntertekNorthAmerica Home Healthcare, IEC 60601-1-11 /slideshow/intertek-webinar-home-healthcare-60601111-1024/27782981 intertekwebinar-homehealthcare60601-1-11-10-131031113336-phpapp01
IEC 60601-1-11 is a mandatory standard provision geared toward determining and documenting failure and hazard potential of medical electrical equipment intended for home use. By addressing the challenges associated with regulating the use of medical devices in the home, we've identified key performance requirements that must be considered when designing a medical device for use outside of the traditional clinical environment.]]>

IEC 60601-1-11 is a mandatory standard provision geared toward determining and documenting failure and hazard potential of medical electrical equipment intended for home use. By addressing the challenges associated with regulating the use of medical devices in the home, we've identified key performance requirements that must be considered when designing a medical device for use outside of the traditional clinical environment.]]>
Thu, 31 Oct 2013 11:33:36 GMT /slideshow/intertek-webinar-home-healthcare-60601111-1024/27782981 IntertekNorthAmerica@slideshare.net(IntertekNorthAmerica) Home Healthcare, IEC 60601-1-11 IntertekNorthAmerica IEC 60601-1-11 is a mandatory standard provision geared toward determining and documenting failure and hazard potential of medical electrical equipment intended for home use. By addressing the challenges associated with regulating the use of medical devices in the home, we've identified key performance requirements that must be considered when designing a medical device for use outside of the traditional clinical environment. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/intertekwebinar-homehealthcare60601-1-11-10-131031113336-phpapp01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> IEC 60601-1-11 is a mandatory standard provision geared toward determining and documenting failure and hazard potential of medical electrical equipment intended for home use. By addressing the challenges associated with regulating the use of medical devices in the home, we&#39;ve identified key performance requirements that must be considered when designing a medical device for use outside of the traditional clinical environment.
Home Healthcare, IEC 60601-1-11 from Intertek
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6 Steps to Global Markets /slideshow/intertek-6-steps-to-global-markets/27782470 intertek-6stepstoglobalmarkets-131031111705-phpapp01
As you start to map out your global strategy beyond the US, Canada and Europe, there are six key steps to follow and multiple regulations to consider. Harmonization has increased in recent years, yet most countries still maintain distinct medical device regulatory systems. Careful analysis on a market-by-market basis will help you to fully realize compliance requirements affecting a particular market. Explore these six steps as we reveal insights into the unique medical device regulations affecting markets in Russia, Brazil, Japan, China, and India.]]>

As you start to map out your global strategy beyond the US, Canada and Europe, there are six key steps to follow and multiple regulations to consider. Harmonization has increased in recent years, yet most countries still maintain distinct medical device regulatory systems. Careful analysis on a market-by-market basis will help you to fully realize compliance requirements affecting a particular market. Explore these six steps as we reveal insights into the unique medical device regulations affecting markets in Russia, Brazil, Japan, China, and India.]]>
Thu, 31 Oct 2013 11:17:05 GMT /slideshow/intertek-6-steps-to-global-markets/27782470 IntertekNorthAmerica@slideshare.net(IntertekNorthAmerica) 6 Steps to Global Markets IntertekNorthAmerica As you start to map out your global strategy beyond the US, Canada and Europe, there are six key steps to follow and multiple regulations to consider. Harmonization has increased in recent years, yet most countries still maintain distinct medical device regulatory systems. Careful analysis on a market-by-market basis will help you to fully realize compliance requirements affecting a particular market. Explore these six steps as we reveal insights into the unique medical device regulations affecting markets in Russia, Brazil, Japan, China, and India. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/intertek-6stepstoglobalmarkets-131031111705-phpapp01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> As you start to map out your global strategy beyond the US, Canada and Europe, there are six key steps to follow and multiple regulations to consider. Harmonization has increased in recent years, yet most countries still maintain distinct medical device regulatory systems. Careful analysis on a market-by-market basis will help you to fully realize compliance requirements affecting a particular market. Explore these six steps as we reveal insights into the unique medical device regulations affecting markets in Russia, Brazil, Japan, China, and India.
6 Steps to Global Markets from Intertek
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https://public.slidesharecdn.com/v2/images/profile-picture.png Let Intertek Clear a Path for your next innovation. Helping manufacturers meet product safety and quality testing requirements around the world since 1896. intertek.com https://cdn.slidesharecdn.com/ss_thumbnails/intertekwebinar-homehealthcare60601-1-11-10-131031113336-phpapp01-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/intertek-webinar-home-healthcare-60601111-1024/27782981 Home Healthcare, IEC 6... https://cdn.slidesharecdn.com/ss_thumbnails/intertek-6stepstoglobalmarkets-131031111705-phpapp01-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/intertek-6-steps-to-global-markets/27782470 6 Steps to Global Markets