Changes to Good Pharmacovigilance Practices in the EU - Webinar By GlobalCompliancePanel 2012
14 Aug 2012
Webinar
Description
Topics
Reporting and Management of Adverse Reactions
Pharmacovigilance systems
Post Authorization Safety Studies
Periodic Safety Update Reports
The Pharmacovigilance Risk Assessment Committee
Changes to Definitions
Who should Attend
Project Managers
Senior Management
PV Reporting
Clinical Trial Heads
Project Managers
Medical Writers
QA / Compliance personnel
CRAs and CRCs
Clinical Research Scientists
Investigators
Consultants
QA / QC Auditors and Staff
Past Events
Changes to Good Pharmacovigilance Practices in the EU - Webinar By GlobalCompliancePanel 2012 - 14 Aug 2012, Webinar (31105)
Changes to Good Pharmacovigilance Practices in the EU 2012 - 20 Jul 2012, Webinar (30540)
Important
Please, check "Changes to Good Pharmacovigilance Practices in the EU - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements
