Software in Medical Devices, by MD101 Consulting - Content of DHF, DMR and DHR for medical device software - Part 3 DHR - 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:md5:9c06172e7cd5ed0f5b192883b657eabbDotclearContent of DHF, DMR and DHR for medical device software - Part 3 DHR - Marimuthu Durn:md5:2c154e6533a914dcf33118ab5e4235752020-07-22T01:12:37+02:002020-07-22T00:12:37+02:00Marimuthu D<p>This is a very useful note about DMR and DHR for me.</p>