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Good Clinical Practice: Sponsor Responsibilities

A one day course aimed at investigators, project managers and associated research team members involved in investigator-led clinical trials, representatives from the pharmaceutical industry and research officers from academic institutions.

This course includes the following content:

  • Clinical Research Governance: Background, Rules and Regulations
  • Principles of Good Clinical Practice
  • Sponsor Responsibilities

HPRA Inspections (Sponsor Perspective)

Date: 17th October 2016

RCSI Education & Research Centre, Smurfit Building, Beaumont Hospital


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