interactive q&a: focus on risk requirements in eu-mdr - april 16th
Published 3 years ago • 296 plays • Length 39:01Download video MP4
Download video MP3
Similar videos
-
12:22
benefit-risk requirements in eu-mdr
-
10:25
iso 14971 & eu-mdr: residual risk requirements
-
58:56
the new eu mdr pms requirements webinar
-
14:55
short course on the medical device regulation (eu) 2017/745
-
1:36:00
the ins and outs of pms requirements under the eu mdr - webinar
-
1:07:09
transitioning from the medical device directives (mdd) to the medical device regulation (mdr)
-
19:43
failure mode and effect analysis (fmea) | quality control tools | lean six sigma tools
-
21:41
post-market surveillance as a medical device requirement in the eu
-
52:10
interactive q&a july 16, 2021: post-market surveillance requirements for medical devices
-
52:52
eu mdr compliance requirements from a vigilance perspective
-
33:32
the essence of the eu mdr
-
50:12
interactive q&a june 11, 2021: post-market surveillance requirements for medical devices
-
1:31:23
taking advantage of the eu mdr delay in uncertain times – celegence webinar
-
1:00:00
webinar | safer medical devices: implementation of the eu mdr and eudamed database
-
46:46
interactive q&a august 20, 2021: post-market surveillance requirements for medical devices
-
0:53
eu mdr transition extension
-
49:50
current challenges in mdr (medical device regulation) in the eu - webinar with no-fear project
-
0:58
who are the new notified bodies?
-
3:25
eu mdr postmarket risk management
-
58:12
a bulletproof clinical evaluation report: making them stand up to regulatory scrutiny
-
5:06
makrocare webinar | risk management - eu mdr perspective
-
0:25
how to prepare for eu mdr