understanding the udi system for medical devices
Published 2 years ago • 780 plays • Length 26:54Download video MP4
Download video MP3
Similar videos
-
4:52
introduction to the udi system in the usa
-
1:08:14
how and when to register eu medical devices and report udi information to eudamed
-
23:30
understanding bill of materials for medical devices
-
38:04
finally, fda finalizes udi requirements document
-
6:41
sys-039 udi requirements procedure
-
1:30:26
understanding the medical device classification system
-
51:59
4 quality system musts for medtech startups to get safe devices to market faster
-
6:09
7 ways to track qms effectiveness using medical device post-market quality processes (track phase)
-
1:29:11
a risk-based approach to qms ahead of iso 13485 changes
-
43:20
udi - us vs eu: what you need to know
-
59:05
understanding the investigational device exemption (ide) process
-
44:48
implementing a global unique device identification (udi) solution: regional update and requirements
-
59:00
understanding global udi rules
-
35:24
understanding fda's new intended use rule and its implications
-
30:09
udi: 101
-
12:36
udi requirements for medical device manufacturers in the eu
-
45:21
greenlight guru virtual summit: economic operators under eu mdr & ivdr
-
47:15
understanding post-market surveillance requirements under eu mdr
-
45:54
key considerations for medical device cloud connectivity
-
41:01
3 systems of medical device risk from fda
-
51:23
ivdr checklist for obtaining ce marking & maintaining eu market access
-
20:27
understanding the basics of unique device identification (udi)