modernizing the eumdr clinical evaluation report process with ethan drower co-founder of citemed
Published 4 months ago • 9 plays • Length 20:00Download video MP4
Download video MP3
Similar videos
-
4:34
introduction to clinical evaluation reports (cer) for europe
-
35:43
what is clinical evaluation under mdr ?
-
45:52
an introductory guide to medical device clinical evaluation & clinical evaluation reports (cer)
-
2:19
clinical evaluation - medical device cers, ceps, literature reviews & data analysis
-
59:52
clinical/performance evaluation for medical device software (mdr ivdr)
-
4:10
5 useful resources when writing a medical device clinical evaluation report (cer)
-
1:08:13
ultimate guide to placing a medical device on the eu market
-
1:05:08
understanding key components of a medical device clinical evaluation
-
13:36
did extension of the eu medical device regulations (mdr) really give you more time?
-
15:58
what is a medical device? (new medical device regulation mdr 2017/745)
-
1:11:19
how to comply to the gspr ? (eu mdr and ivdr - monir el azzouzi)
-
13:14
clinical evaluation of medical devices prior and after mdr
-
58:33
cer critical concepts: effectively telling the story of the clinical evaluation report
-
6:58
what is the eu mdr ? l the learning reservoir
-
1:01:30
raps sponsored webinar: understanding key components of a clinical evaluation
-
37:09
how to perform product equivalence on your cer (clinical evaluation report)?
-
16:55
how to update your clinical evaluation report (cer) for 2024
-
![ai act vs. eu mdr 2017/745 are they compatible? [erik vollebregt]](https://i.ytimg.com/vi/bx7d_Jf6JL8/mqdefault.jpg)
34:54
ai act vs. eu mdr 2017/745 are they compatible? [erik vollebregt]
-
1:29:01
clinical evaluations for unique product types under the eu mdr – webinar
-
19:45
how to prepare your medical device or ivd for clinical evaluation