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Adverse Event Reporting November 2011
22-23 Nov 2011
MWB Victoria, London, United Kingdom
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Adverse Event Reporting November 2011
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Description
Adverse Event Reporting November 2011
will cover the following topics:
Periodic safety update reports (PSUR)
Global harmonisation: ICH and CIOMS
Adverse event reports
EU requirements
Key signals for preventive actions
Accurate causality assessment to identify the origin of ADRs
Post-marketing issues and drug sales revenue
Monitoring drug reactions to avoid negligence blames
Past Events
Adverse Event Reporting November 2011 - 22-23 Nov 2011, MWB Victoria, London, United Kingdom
(15758)
Adverse Event Reporting September 2011 - 15-16 Sep 2011, Prague, Czech Republic
(15757)
Adverse Event Reporting July 2011 - 26-27 Jul 2011, MWB Victoria, London, United Kingdom
(15756)
Important
Please, check "Adverse Event Reporting" official website for possible changes, before making any traveling arrangements
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Pharma
Science:
Life Sciences & Biology
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