Research Governance Training
It is the policy of both Queen Mary and Barts Health that all researchers conducting research at our sites must attend appropriate training. It is mandated that all researchers of MHRA-regulated trials must complete a GCP course and refresh within the preceding three years. The same is advised as the best practice for all other researchers.
More details regarding research-specific training can be found in JRMO SOP 34a Researcher Training and SOP 12b Barts Health/Queen Mary Sponsorship of Interventional Studies Process for JRMOs staff [PDF 317KB]
Booking research governance training
To book a course please email research.governance@qmul.ac.uk with the subject title 'GCP COURSE BOOKING' and include, in the body of the email, the name and date of the JRMO course you wish to attend (see below). Your place will be confirmed by email.
GCP for Lab Staff courses are not being run this term. Please contact research.governance@qmul.ac.uk for more information.
Courses for Queen Mary or Barts Health staff members only |
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Title
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Date
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Time
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Delivery
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| GCP Refresher | Mon 7 Sep 2026 | 09.30 - 12.00 | MS Teams |
| Implementation of GCP at Barts Health NHS Trust and Queen Mary University of London | Mon 5 Oct 2026 | 09.30 - 13.00 | MS Teams |
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GCP Refresher |
Thu 5 Nov 2026 |
09.30 - 12.00 |
MS Teams |
| GCP for Clinical Investigations ISO14155 |
Wed 11 Nov 2026 |
13.30 - 16.30 |
MS Teams |
| GCP Refresher |
Thu 10 Dec 2026 |
13.30 - 16.00 |
MS Teams |
Courses available to Queen Mary, Barts Health or North Thames RRDN staff |
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Title
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Date
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Time
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Delivery
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Governance training: |
Not running Sept – Dec 2026 Please email for interested list |
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Booking Human Tissue Act training
Bookings can be made via contacting the HTRC Manager or via QMUL CPD platform
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Title
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Date
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Time
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Delivery
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| Human Tissue Act and the Implications for Research - Introduction course |
2nd July 2026 5th October 2026 3rd December 2026 |
2-3pm | MS Teams |
| Human Tissue Act and the Implication for Research - Refresher course |
14th September 2026 5th November 2026 |
2-3pm | MS Teams |
UK clinical trials regulations training
'Preparing for audits and inspections' session
Are you ready for an inspection? Not sure how to prepare for an upcoming audit?
Laura Vosper (Quality Assurance Manager, CECM) and Amy Schou (Clinical Trials Auditor, JRMO) will be running a session preparing audits and inspections.
Both have experience in inspections from the MHRA, HTA, and FDA. In session, they will talk about how to prepare for audits and inspections from both a location and sponsor perspective
Join them on Weds 11th Nov 2026, from 12:00-13:00 pm.
To join online, click on this link, or complete this form to receive a calendar invitation.