Software in Medical Devices, by MD101 Consulting - Read me firstBlog about software medical devices and their regulatory compliance. Main subjects are software validation, IEC 62304, ISO 13485, ISO 14971, CE mark 93/42 directive and 21 CFR part 820.2024-03-18T07:25:39+01:00Cyrille Michaudurn:md5:9c06172e7cd5ed0f5b192883b657eabbDotclearCC-BY-NC-ND Licenseurn:md5:e524322c37de137ae06899d08e53b35f2011-10-03T13:01:00+02:002014-10-13T11:40:45+02:00MitchRead me first <p>The content of this website is the property of Cyrille Michaud.<br />
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