understanding the intricacies of the finalized eu ivd and medical device regulation
Published 7 years ago • 174 plays • Length 2:50Download video MP4
Download video MP3
Similar videos
-
14:55
short course on the medical device regulation (eu) 2017/745
-
28:50
webinar: a regulatory q&a with ivd expert robyn meurant
-
1:03:08
understanding the in vitro diagnostic regulation (ivdr) everything you need to know
-
4:12
regulatory fundamentals of medical devices in the eu (part 1)
-
5:43
overview of the new eu- in-vitro diagnostics regulation.
-
46:34
eu battery regulation 2023/1542 – how to be ready for medical device companies?
-
1:11:19
how to comply to the gspr ? (eu mdr and ivdr - monir el azzouzi)
-
1:05:19
how to build a winning strategy for eu mdr compliance & medical device regulatory requirements
-
4:12
global medical device registration impact of changes to the eu mdr and chinese gcp on manufacturers
-
34:10
medtech summit 2020 | eu medical device regulation, notified body overview and update from bsi
-
12:36
udi requirements for medical device manufacturers in the eu
-
10:43
eu medical device and diagnostic regulatory overhaul: the regulatory implications
-
5:14
in vitro diagnostic regulations eu 2017/746 - what are they?
-
52:23
navigating the in vitro diagnostic regulation (ivdr) rollout for legacy & new devices - webinar
-
2:43
the uk vs the eu medical device regulations - what are the key differences?
-
16:51
upcoming revisions of eu regulations & the reclassification of in vitro diagnostics
-
22:58
overview of eu regulations for in-vitro diagnostic medical devices
-
8:01
the future of medical device regulation in the european union – europcr 2019
-
1:43
why you need an eu medical device importer
-
37:15
changing requirements for manufacturers under ivdr
-
5:29
understanding the role of the prrc for medical devices and ivds in the eu | patient guard
-
3:27
hear about the changes to the eu mdr and ivdr and the future of the medical device industry