Due to the cessation of face-to-face teaching on QMUL campuses, some changes have been made to the current provision. Check the Venue column for information. Sessions will either proceed online at their scheduled times or will be POSTPONED with further notice. Please check your email as you will likely have received notice, or contact your tutor for more information | Introduction of new booking system

Course Detail

GCP003 - Good Clinical Practice (GCP) Refresher

This course is suitable for researchers who have previously attended GCP training but need to refresh and update their knowledge. The course is suitable for all clinical research, including Clinical Trials of Investigational Medicinal Products (CTIMPs). If you have not attended GCP training before, please book on to the Good Clinical Practice Full Course or Good Clinical Practice for non-CTIMP Research.
It is mandatory that researchers working on CTIMPS at Queen Mary University of London or Barts Health NHS Trust attend this course every two years.

Summary
This two and a half hour course aims to refresh attendees’ knowledge of Good Clinical Practice, the UK regulations and sponsor requirements. The course will review the principles of Good Clinical Practice, the UK Policy Framework for Health and Social Care Research and the Clinical Trial Regulations and describe how they should be applied to Barts Health /Queen Mary sponsored clinical research.

Fees
This course is available free of charge for at staff who work for Queen Mary and Barts Health. External attendees should contact cpd@qmul.ac.uk prior to registering to discuss costs.

Please note:
I will be sending diary invites (email addresses will be seen). Please ensure your account is registered with NHS or QMUL email addresses.

We will send the presentation handout prior to the course as we are reducing our printing output across the university.

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 1 April 2020

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

Time: 13:30 - 16:00


Tutor

  • Mrs M Good