how to work with annex viii from the medical device regulation (eu mdr)
Published 3 years ago • 461 plays • Length 4:29Download video MP4
Download video MP3
Similar videos
-
4:57
how to work with annex i from the medical device regulation (eu mdr)
-
14:55
short course on the medical device regulation (eu) 2017/745
-
1:05:19
how to build a winning strategy for eu mdr compliance & medical device regulatory requirements
-
32:47
introduction to the european medical devices regulation mdr eu 2017 745
-
38:18
how to become the best prrc ever? [eu mdr & ivdr]
-
1:11:19
how to comply to the gspr ? (eu mdr and ivdr - monir el azzouzi)
-
17:40
medical device regulation codes
-
58:56
the new eu mdr pms requirements webinar
-
1:03:18
understanding europe's medical device regulation
-
1:12:50
technical documentation for medical devices webinar
-
6:51
why is it awesome to work in quality and regulatory affairs? (medical devices)
-
33:57
how to create a quality management system compliant to mdr and ivdr?
-
16:51
upcoming revisions of eu regulations & the reclassification of in vitro diagnostics
-
2:41
what is mdr compliance?
-
47:54
how to deal with the new post-market surveillance requirements under regulation (eu) 2017/745
-
22:19
implant card requirements for article 18 of eu mdr
-
20:38
how to deal with significant changes for your medical devices (eu mdr)
-
1:03:09
the best tips to build an mdr / ivdr project? (medical device regulation)
-
4:10
5 useful resources when writing a medical device clinical evaluation report (cer)
-
35:37
i want to become a prrc with team-prrc (eu mdr & ivdr)
-
23:24
eu exit and post-transition guidance, regulation of medical devices webinar - october 2020