How Accurate Adverse Event Reporting is the Key to Subject Safety of Approved Drugs

Description

How Accurate Adverse Event Reporting is the Key to Subject Safety of Approved Drugs is a webinar that covers topics such as:

  • How to know what an Adverse Event is and when to report it or them
  • The definitions of Adverse Events, Serious Adverse Events, Unanticipated Adverse Device Effects and many more
  • Understanding laboratory AEs and the "Reference Range" concept
  • Knowing the AE types and likelihood of finding "rare" events
  • Reporting of Adverse Events - when and to whom and the use of AE Terminology systems
  • Common Mistakes in AE / SAE Reporting
  • How to record Adverse Events and assess causality - the algorithm

How Accurate Adverse Event Reporting is the Key to Subject Safety of Approved Drugs is intended for:

  • Clinical Research Scientists
  • Principal Investigators and Sub Investigators
  • Clinical Research Associates (CRAs) and Coordinators (CRCs)
  • Safety Nurses
  • Clinical Research Data Managers
  • QA / QC Auditors and Staff

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Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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