ADVERSE EVENT MANAGEMENT DURING MEDICAL DEVICE CLINICAL STUDIES IN EUROPE 2012

  • 27 Jan 2012
  • Cavendish Hotel, London, United Kingdom

Description

Topics
  • Adverse event forms
  • Regulations governing the monitoring and reporting of adverse events
  • Adverse events definition and classification

Past Events

Important

Please, check "ADVERSE EVENT MANAGEMENT DURING MEDICAL DEVICE CLINICAL STUDIES IN EUROPE" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device

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