Software in Medical Devices, by MD101 Consulting - MHRA guidance about standalone 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 820.2024-03-18T07:25:39+01:00Cyrille Michaudurn:md5:9c06172e7cd5ed0f5b192883b657eabbDotclear