01 Mar

21 CFR 820 to ISO 13485:2016

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08 Jan

IEC 60601-1-2 4th Edition: Are You Ready?

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04 Jan

New FDA Guidance for Interoperable Medical Devices

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04 Jan

The Demand for Connectivity

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29 Nov

RoHS Directive 2011

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20 Nov

Transitioning Your Quality System – ISO13485:2016

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20 Sep

Is Your Software a Medical Device?

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10 Jul

Medical Device Software Development Lifecycle Standard Changes – IEC 62304:2006 vs. 62304:2015 (Amendment 1)

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05 Jul

FDA Product Safety Standard Deadline Looming – 60601-1 Edition 3, Amendment 1

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20 May

The Realtime Group Announces New Facility Open House

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