the abcs of medical device software compliance under eu regulations 2017/745 and 2017/746 - webinar
Published 1 year ago • 443 plays • Length 1:01:39Download video MP4
Download video MP3
Similar videos
-
14:55
short course on the medical device regulation (eu) 2017/745
-
38:08
software as a medical device classification rule 11 (eu mdr 2017/745)
-
48:15
how to choose your prrc ? (eu mdr 2017/745 - ivdr 2017/746)
-
20:34
is my product a medical device in europe ? (eu mdr 2017/745)
-
1:05:21
is my software a class i medical device? [eu mdr 2017/745]
-
1:07:09
transitioning from the medical device directives (mdd) to the medical device regulation (mdr)
-
50:27
how to do post marketing surveillence in the us? (vs europe)
-
1:03:18
understanding europe's medical device regulation
-
50:28
clinical evidence for medical devices under regulation (eu) 2017/745
-
7:22
how to market a custom-made medical device? (eu mdr 2017/745)
-
21:16
preparation for the in vitro diagnostic regulation ivdr 2017/746
-
32:47
introduction to the european medical devices regulation mdr eu 2017 745
-
10:53
medical device regulation transition timeline (mdr 2017/745)
-
34:22
how to make labelling regulatory compliant for eu-mdr (2017/745)
-
40:58
webinar - process & technology innovation in eu mdr compliance
-
3:31:37
ema webinar on article 117 of the medical devices regulation eu 2017/745
-
59:52
clinical/performance evaluation for medical device software (mdr ivdr)
-
1:05:04
celegence eumdr webinar - how to start preparing your ra qa team for the eudamed database
-
1:36:00
the ins and outs of pms requirements under the eu mdr - webinar
-
1:11:19
how to comply to the gspr ? (eu mdr and ivdr - monir el azzouzi)
-
57:11
webinar // cybersecurity in the medical devices – how to show compliance to regulatory requirements
-
47:54
how to deal with the new post-market surveillance requirements under regulation (eu) 2017/745