Investigator Reporting Responsibilities: AEs, Unanticipated Problems, Modifications, and Deviations 2018

  • 18 May 2018
  • Webinar

Description

Topics
  • Overview of recent changes in regulatory framework
  • FDA Regulations
  • FDA guidance on electronic source documentation
  • GCP R2 Guidelines
  • Quality Management of Data
  • FDA BIMO Program
  • Enhancing Excellence in conduct of Clinical Trials
Who should Attend
  • Clinical Research Associates (CRAs)
  • Research Managers
  • Compliance Officers
  • Clinical Research Coordinators

Past Events

Important

Please, check "Investigator Reporting Responsibilities: AEs, Unanticipated Problems, Modifications, and Deviations" official website for possible changes, before making any traveling arrangements

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Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical laboratories, Medical technology

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