Software in Medical Devices, by MD101 Consulting - How to differenciate Bugs, Software Risks and Software Failures - Part 1 - 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:md5:9c06172e7cd5ed0f5b192883b657eabbDotclearHow to differenciate Bugs, Software Risks and Software Failures - Part 1 - Ike Siposurn:md5:fd527310bd5a50f0e7b5af3bee2f3b5a2017-12-19T17:13:24+01:002017-12-28T21:19:01+01:00Ike Sipos<p>Amen for this immensely informative blog. Software bugs can be one of the most infuriating aspects of development. Not to mention the negative backlash that ensues when clients are unhappy. I cherished the level of detail you go into. Thanks again.</p>