Course Detail

GCP003 (GCP Refresher) - Good Clinical Practice (GCP) Refresher

This course is suitable for those who are working on Clinical Trial of Medicinal Products (CTIMPs/drug trials) who have previously attended GCP training but need to refresh and update their knowledge. This course is mandatory for all researchers working on CTIMPs every two years. This course is available for all staff who work for Queen Mary’s University of London and Barts Health NHS Trust, and will not be charged for. Delegates must register before the course and will be issued a certificate upon completion of the course.

This two hours course will refresh and update the knowledge of those working on Clinical Trials of Medicinal Products (CTIMPs/drug trials) of Good Clinical Practice and Clinical Trial Regulations and how to apply them in their role.

Objectives

By the end of this course, participants should be able to:

  • Refresh clinical trial research staff's knowledge of Clinical Trial Regulations and Amendments
  • Refresh clinical trial research staff's knowledge of the requirements to comply with the protocol, agreements and approvals
  • Refresh clinical trial research staff's knowledge of Informed Consent
  • Refresh clinical trial research staff's knowledge of Compliance with the Data Protection Act and Human Tissue Act
  • Refresh clinical trial research staff's knowledge of Safety Reporting

Provided by: Joint Research Management Office

Details

Date: Wednesday 20 March 2019

Venue: Clark Kennedy Lec Theatre, W, Queen Mary Innovation Centre, Whitechapel

Time: 14:00 - 16:30


Tutor

  • Mrs M Good