Intermediate Level Adverse Event Reporting 2011

  • 14-15 Apr 2011
  • MWB Victoria, London, United Kingdom

Description

The growing awareness of the size and severity of adverse drug reactions, especially with the global use of medicines, has highlighted the need to streamline adverse event reporting and get the right information in the right format as quickly as possible.

This advanced-level course will provide decision-makers with the training and knowledge essential to cope with the demands of pharmacovigilance. Packed full with practical exercises and case studies, there can be no better way to ensure that you and your colleagues act competently and confidently throughout the drug safety process.

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Important

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

Event Categories

Business: Quality assurance, Security & Safety
Health & Medicine: Pharma
Technology: Data management

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