Monitoring – how to make it pain-free (well, almost)

Start Date/Time:
30 October 2017 09:30
End Date/Time:
30 October 2017 12:30
Location:
School of Cancer Sciences- University of Birmingha
Venue:
Room 127, Cancer Research UK Clinical Trials Unit, Institute of Cancer & Genomic Sciences, Universit

Target Audience: Suitable for any members (new or experienced) of the research site staff team (e.g. Data Managers, Research Nurses, Trial Coordinators) who facilitate on-site monitoring visits.

Aims and Objectives: On-site monitoring of clinical trials is all about ensuring patient safety and data quality. This interactive workshop aims to

  • Explain the monitoring process – what do the Monitors do and why?
  • Highlight common monitoring and inspection findings
  • Provide an opportunity to share best practice and explore strategies to avoid findings

Course Summary: This study session aims to give participants an understanding of the monitoring process – what do the Monitors do and why?; some common monitoring and inspection findings and some strategies to avoid findings

On 14 June 2017