Software in Medical Devices, by MD101 Consulting - Happy New Year 2017 - CommentsBlog 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 820.2024-03-27T15:32:28+01:00Cyrille Michaudurn:md5:9c06172e7cd5ed0f5b192883b657eabbDotclearHappy New Year 2017 - Benurn:md5:408eacadc69bea892f108c81c2b9e11a2017-01-03T10:41:37+01:002017-01-03T10:41:37+01:00Ben<p>Happy New Year, Mitch.</p>
<p>Look forward to reading your insights this year, especially as we get closer to the final publications of the MDR and IVDR.</p>
<p>(Have you had chance to digest the 21st Century Cures Act?)</p>