How Accurate Adverse Event Reporting is the Key to Subject Safety of Approved Drugs 2018

  • 06 Feb 2018
  • Webinar

Description

How Accurate Adverse Event Reporting is the Key to Subject Safety of Approved Drugs 2018 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 2018 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

Past Events

Important

Please, check "How Accurate Adverse Event Reporting is the Key to Subject Safety of Approved Drugs" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Pharma

Other Events with Similar Categories

Other Events with Similar Location or Organizer

Featured Conferences & Exhibitions