Please Note:

Course Detail

GCP003 - Good Clinical Practice (GCP) Refresher

UPDATED Aug 2020 - Due to the pandemic we continue to put interim measures in place to deliver the Good Clinical Practice course with shorter more concise tutorials on the local Barts Health and Queen Mary requirements, updates and hot topics.

You will receive a diary invite for access to the tutorial - please use QMUL or nhs.net email addresses as your email address will be visible. If there are any problems, please contact Rhona Atkin, Clinical Trials Facilitator in JRMO on Rhona.atkin@qmul.ac.uk who is setting up the diary invites.
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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.

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. If you are unsure which course is best for your research, please contact Rhona Atkin, Clinical Trials Facilitator in JRMO on Rhona.atkin@qmul.ac.uk.

Summary
This two-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.

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: Thursday 15 October 2020

Venue: Online - MSTeams, Microsoft Teams Meeting, Web/Online

Time: 14:00 - 16:30


Tutor

  • Mrs M Good