us postmarket surveillance requirements for medical devices
Published 1 year ago • 1.2K plays • Length 57:13Download video MP4
Download video MP3
Similar videos
-
1:25:47
eu postmarket surveillance requirements for medical devices
-
1:37
purpose of the post-market surveillance process for medical devices
-
21:41
post-market surveillance as a medical device requirement in the eu
-
46:46
interactive q&a august 20, 2021: post-market surveillance requirements for medical devices
-
50:12
interactive q&a june 11, 2021: post-market surveillance requirements for medical devices
-
1:30:28
post-market surveillance for medical devices & combination products
-
47:54
how to deal with the new post-market surveillance requirements under regulation (eu) 2017/745
-
1:24
post market surveillance for medical devices
-
52:10
interactive q&a july 16, 2021: post-market surveillance requirements for medical devices
-
50:27
how to do post marketing surveillence in the us? (vs europe)
-
7:19
sys-019 post-market surveillance procedure and templates
-
2:16
webinar: how to set up post-market surveillance for your medical device
-
11:33
is human factors engineering part of post-market surveillance?
-
13:18
post-market surveillance for medical device industries in the eu: responsibilities and obligations
-
2:33
intelligent post-market surveillance for medical devices
-
5:19
post-market surveillance summary reporting webinar
-
13:45
what’s missing from your post-market surveillance plan?