28:57
How to Manage Global LSO/Local QPPV Requirements
32:09
Globalisation of QP Requirements
32:09
QPPV and local requirements
29:48
Unlock the Secrets of the EU Marketing Authorization Application
28:20
Risk Minimisation
36:24
Tip tips for report writing in pharmacovigilance
32:41
Signal Detection in PV
36:47
Literature Monitoring and Review
36:17
Post Authorisation Safety
33:50
Medication Errors
37:02
Device Vigilance in PV
36:39
GVP Modules
36:57
The Importance of the Quality Management System
33:53
Types of pharmacoepidemiological studies and what their biases may be
32:21
Causality Assessments
22:10
Compliant & Effective Market Research Results
40:24
Understanding the GVP Module V
18:15
Advisory Board Meeting
43:41
Signal Detection and Eudravigilance
43:58
Case Processing and Eudravigilance
33:25
Reference Safety Information
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27 March 2015
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