how to lead a mdr or ivdr project without issue (pitfalls)
Published 4 years ago • 1.1K plays • Length 13:59Download video MP4
Download video MP3
Similar videos
-
38:18
how to become the best prrc ever? [eu mdr & ivdr]
-
1:03:09
the best tips to build an mdr / ivdr project? (medical device regulation)
-
35:37
i want to become a prrc with team-prrc (eu mdr & ivdr)
-
29:50
how to create your medical device technical file [eu mdr & ivdr]
-
16:44
how to find a notified body for eu mdr or ivdr
-
29:03
the step-by-step method to get mdr - ivdr certified
-
11:02
mdr & ivdr
-
33:57
how to create a quality management system compliant to mdr and ivdr?
-
15:40
format & content of a medical device file (mdf) - iso 13485:2016, clause 4.2.3
-
1:20:11
preparing your technical documentation under mdr: proven tips & techniques
-
44:08
demonstrating conformity to general safety and performance requirements gspr under mdr
-
59:52
clinical/performance evaluation for medical device software (mdr ivdr)
-
1:01
understanding the mdr & ivdr: what medical device companies need to know.
-
1:11:19
how to comply to the gspr ? (eu mdr and ivdr - monir el azzouzi)
-
49:50
current challenges in mdr (medical device regulation) in the eu - webinar with no-fear project
-
43:29
webinar we're off! implementing the european mdr and ivdr with recordings
-
7:22
how to market a custom-made medical device? (eu mdr 2017/745)
-
48:15
how to choose your prrc ? (eu mdr 2017/745 - ivdr 2017/746)
-
56:52
critical concepts: deep dive into mdr and ivdr device classification and data collection strategies
-
34:48
medical device news - october 2021 regulatory update
-
33:43
mdr and ivdr discussion with erik vollebregt part 2 (medical devices)