bsi medical devices | a full scope notified body under the eu ivdr
Published 1 year ago • 509 plays • Length 1:51Download video MP4
Download video MP3
Similar videos
-
34:10
medtech summit 2020 | eu medical device regulation, notified body overview and update from bsi
-
29:41
bsi medical devices | ivdr class d requirements in the absence of eu reference laboratories
-
1:54
bsi medical devices | ivdr timeline
-
2:28
bsi medical devices | mapping regulations ivdr
-
0:44
bsi medical devices | mdsap
-
4:45
bsi compliance navigator | mdr and ivdr – key changes
-
2:11
bsi 醫療器材│歐盟醫療器材法規 mdr 指引─part 1 後脫歐和 mdr 第二修正案
-
10:01
bsi medical devices | guide to conformity
-
2:01
bsi medical devices | mapping regulations mdr
-
2:19
bsi medical device safety: understanding en 60601 standard
-
1:57
#ivdronair video series: ivdr applications lessons learnt
-
1:03:08
understanding the in vitro diagnostic regulation (ivdr) everything you need to know
-
4:14:50
: bsi-aami international standards & regulations conference - day 1
-
3:54
bsi medical devices | end of year message from manuela gazzard 2022
-
32:12
i help you select your notified body & understand the full process
-
52:23
navigating the in vitro diagnostic regulation (ivdr) rollout for legacy & new devices - webinar
-
1:01
understanding the mdr & ivdr: what medical device companies need to know.
-
57:54
medical device regulation: perspectives of a notified body with innoscot health