Software in Medical Devices, by MD101 Consulting - V&V: verification & validation, doing it right. - 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:md5:9c06172e7cd5ed0f5b192883b657eabbDotclearV&V: verification & validation, doing it right. - Loïc Fejozurn:md5:f48bdc90e307c159b98060302e010a2f2012-11-16T15:25:01+01:002012-11-16T15:25:01+01:00Loïc Fejoz<p>About definition of Verification and validation, and more generaly for definition in the field of design and system building, it is interested to have a look at the SEBoK (Systems Engineering Book of Knowledge) glossary. They aggregate several definition in one place.</p>
<p>See<br />
<a href="http://www.sebokwiki.org/1.0/index.php/Validation_%28glossary%29" title="http://www.sebokwiki.org/1.0/index.php/Validation_%28glossary%29" rel="ugc nofollow">http://www.sebokwiki.org/1.0/index....</a><br />
<a href="http://www.sebokwiki.org/1.0/index.php/Verification_%28glossary%29" title="http://www.sebokwiki.org/1.0/index.php/Verification_%28glossary%29" rel="ugc nofollow">http://www.sebokwiki.org/1.0/index....</a></p>
<p>Note that you would probably find some interesting materials in the SWEBoK (Software Engineering Book of Knowledge).</p>
<p>Anyway your article is a good reminder for everyone...</p>