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
See location on maps.ox

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
This talk features in the following public collections:
- Talks of Interest to Medical Sciences
- Oxford Neuroscience Seminar List
Editor: Mark Crossley