medical device complaint handling systems
Published 8 years ago • 2.3K plays • Length 1:09:52Download video MP4
Download video MP3
Similar videos
-
1:04:54
complaint handling in compliance with fda and iso regulations
-
1:00:35
medical device complaint handling: mdr, reports of removals and corrections
-
0:16
medical device complaint handling
-
30:25
complaint handling with medical device guru, brittney mciver
-
3:43
complaint handling and reporting process for medical devices
-
3:38
complaint files 820.198 & iso 13485 § 8.2.1 – 8.2.3 (executive series #27)
-
51:00
regulatory standards & risk management in medical devices
-
5:40
understanding the three stages of process validation
-
1:02:57
design history file dhf, device master record dmr, device history record dhr and technical file tf
-
1:17:25
conducting successful product complaint investigations
-
10:10
conducting successful product complaint investigations - globalcompliancepanel
-
1:12:06
medical devices - iso 14971 : risk management
-
1:28:00
process validation for medical device manufacturers
-
11:01
capa challenges and fda expectations - globalcompliancepanel
-
1:05:37
managing the medical device supply chain
-
1:17:36
recalls, corrections and removals (devices)
-
1:16:37
cgmp for medical devices including ivds
-
1:06:19
recalls, removals, and market corrections in compliance with fda and iso requirements
-
59:53
medical device design control
-
39:23
fda's current thinking on cgmp compliance for phase i investigational drug and biologic products
-
1:02:57
fda quality systems regulation requirements - regulatory documents explained