managing the eu mdr with electronic data capture (edc)
Published 4 years ago • 787 plays • Length 1:04Download video MP4
Download video MP3
Similar videos
-
20:47
managing clinical trials utilizing electronic data capture edc2 2021
-
58:56
the new eu mdr pms requirements webinar
-
1:00:00
webinar | safer medical devices: implementation of the eu mdr and eudamed database
-
50:04
how electronic data capture is transforming the medtech industry
-
21:41
post-market surveillance as a medical device requirement in the eu
-
43:29
webinar we're off! implementing the european mdr and ivdr with recordings
-
38:08
software as a medical device classification rule 11 (eu mdr 2017/745)
-
1:08:13
ultimate guide to placing a medical device on the eu market
-
5:23
what is the eu medical devices regulation (mdr)?
-
2:27
researchmanager edc - electronic data capture system to capture clinical data fast & safe
-
12:22
benefit-risk requirements in eu-mdr
-
2:25
conducting studies using electronic data capture
-
4:07
follow the patient: electronic data capture - presenting, screening & operative
-
1:29:01
clinical evaluations for unique product types under the eu mdr – webinar
-
33:57
how to create a quality management system compliant to mdr and ivdr?
-
4:14
smart technology enables a holistic, data-driven approach to eu mdr/ivdr
-
1:10:58
eu mdr: how do i interpret the new regulations and what do i need to do to be compliant?
-
1:30
what is a clinical electronic data capture (edc) system?
-
22:19
implant card requirements for article 18 of eu mdr
-
56:59
mdr effects on medical device processing