Adverse Event Reporting November 2011

  • 22-23 Nov 2011
  • MWB Victoria, London, United Kingdom

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

Important

Please, check "Adverse Event Reporting" official website for possible changes, before making any traveling arrangements

Event Categories

Education: Training
Health & Medicine: Pharma
Science: Life Sciences & Biology

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