Software in Medical Devices, by MD101 Consulting - IEC 62366-1 and Usability engineering for software - 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:md5:9c06172e7cd5ed0f5b192883b657eabbDotclearIEC 62366-1 and Usability engineering for software - Hobberurn:md5:749d11257d378959cda79a8ff4aa360b2019-12-17T13:07:26+01:002019-12-17T13:07:26+01:00Hobber<p>That was really useful, thx a lot. You explained the human, knowhow side of doing it, that others don't.</p>