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Introduction to GCP. (Good Clinical Practice). This training is intended for University & NHS research staff involved in clinical research falling under the Clinical Trials Regulations.
Status: This talk is in preparation - details may change
An introduction to GCP
Legislation including Data Protection, Human Tissue Act
Sponsor, funder, host organisation, CI
Documents required before study start – Approval, SOPs, Trial Master File, contracts
Conducting the trial
Eligibility, informed consent, IMP & data management, safety reporting
Monitoring, audit, reports, ongoing responsibility
Web resources
Responsibilities
Date:
30 July 2019, 9:30
Venue:
Boundary Brook House, Churchill Drive, Headington OX3 7LQ
Venue Details:
Magdalen Conference Room
Speakers:
Nigel Wellman (University of Oxford),
Jo Franklin (Oxford University Hospitals NHS Foundation Trust),
Dr Kate O'Neill (University of Oxford)
Organising department:
Research Services
Organiser:
Mark Crossley (University of Oxford - CTRG)
Organiser contact email address:
mark.crossley@admin.ox.ac.uk
Booking required?:
Required
Booking email:
mark.crossley@admin.ox.ac.uk
Cost:
N/A
Audience:
Members of University of Oxford and OUH NHS Foundation Trust only
Editor:
Mark Crossley
