what is the safer technologies program (step) and can your device use it?
Published 3 years ago • 413 plays • Length 33:17Download video MP4
Download video MP3
Similar videos
-
40:43
comparing fda’s breakthrough devices program & safer technologies program
-
7:34
integrating design controls & risk management to streamline product development (make phase)
-
45:54
key considerations for medical device cloud connectivity
-
49:37
how to accelerate product development with ux design & human factors engineering
-
35:14
digitizing your samd testing
-
50:28
why design validation is more than testing: how to validate your validation
-
47:00
how to get covid-19 devices to market using fda emergency use authorization (eua) program
-
52:32
iso 14971:2019 & tr 24971 explained - medical device risk management
-
1:30:28
post-market surveillance for medical devices & combination products
-
1:01:30
the importance of computer system validation for regulated systems
-
59:05
understanding the investigational device exemption (ide) process
-
44:46
emdr program and process
-
44:48
implementing a global unique device identification (udi) solution: regional update and requirements
-
47:57
what to expect during medical device remote audits
-
47:26
recent fda feedback regarding extractable and leachable testing
-
29:30
overcoming barriers to receiving 510k clearance
-
34:45
business risk management for medical device companies
-
45:27
qms from a regulatory perspective
-
45:16
post covid-19 value shift & how medtech companies can capitalize
-
44:30
what "exempt" means with respect to medical devices & regulatory
-
50:04
how electronic data capture is transforming the medtech industry