fda adverse event reporting system (faers) overview - pharmacovigilance 2020
Published 4 years ago • 7.5K plays • Length 48:21Download video MP4
Download video MP3
Similar videos
-
55:59
submitting ind safety reports to fda adverse event reporting system (faers)- nov. 1, 2019
-
59:21
electronic submission of adverse event reports to faers using ich e2b(r3) standards - oct. 11, 2019
-
54:27
fda's sentinel initiative - pharmacovigilance 2020
-
32:55
upgrading the fda adverse event reporting systems - faers
-
43:22
live demo of the fda adverse events reporting system (14/14) redi 2017
-
27:21
digital ind safety reporting - pharmacovigilance 2020
-
30:38
keynote – pharmacovigilance and risk management conference 2020
-
9:23
the fda's adverse event reporting system (faers) public dashboard
-
35:16
overview of postmarketing drug safety reporting requirements - redi 2020
-
0:33
fda adverse events reporting system (faers) showcase
-
41:06
division of risk management: overview of review activities and rems - pharmacovigilance 2020
-
32:55
upgrading the fda adverse event reporting system (faers)
-
34:57
icsr data quality of coding: products, adverse events and medication errors - pharmacovigilance 2020
-
5:52
questions and discussion – pharmacovigilance 2020
-
10:01
pharmacoviligance analysis with the fda adverse event reporting system
-
42:22
development of shared system rems & implications of the appropriations act - pharmacovigilance 2020
-
23:33
combination products: reporting device information and malfunctions - pharmacovigilance 2020
-
48:56
naltrexone injection for opioid use disorder: fda's efforts to reduce medication errors
-
38:16
considerations for rems surveys and assessments: planning and reporting - pharmacovigilance 2020