Face-to-Face Good Clinical Practice (GCP) Training
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Note: To be eligible for registration on these courses, you must be employed either by Oxford University or the Oxford University Hospitals NHS Trust. All training will take place in the Joint Research Office, Meeting Room 1, Churchill Hospital. |
- GCP for Clinical Trials of Investigational Medicinal Products (CTIMPs) as defined by the Clinical Trials Regulations
- GCP for Clinical Research Studies (i.e. studies not falling under the Clinical Trials Regulations)
- How to Book
GCP for Clinical Trials of Investigational Medicinal Products (CTIMPs) as defined by the Clinical Trials Regulations
New format from 2012 onwards
The compulsory module will be around 5.5 hours and the additional modules will take about 1.5 hours.
The Core Module will act as the Refresher for those who require updated training.
Compulsory Core Module intended for ALL staff working on CTIMPs
- 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, On Going Responsibility - Web Resources
- Responsibilities
Additional Modules
Module 1: Trial Design intended for PIs or those writing protocols
- Protocol Development
- Writing associated documents
- Funding
- Responsibilities of CI & Sponsor
- Sponsorship
Module 2: Submission for approvals for anyone responsible for preparing submissions
- Applications to REC, MHRA, NHS Permission
Dates
| Module | Dates | Time |
|---|---|---|
| Addit. Module 1 (Trial design) |
27-Sep-13 2-Dec-13 |
12-2 pm 12-2 pm |
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Addit. Module 2 (Document preparation for submission) |
30-Sep-13 5-Dec-13 |
12-2 pm 12-2 pm |
| Compulsory Core Module |
16-Sep-13 25-Nov-13 13-Dec-13 |
9 am-4 pm (full) 9 am-4 pm (full) 9am-4 pm |
Further Information
For details on which (if any) of the additional modules you may wish to attend please contact Karl Shepherd on 01865 572221.
GCP for Clinical Research Studies (i.e. studies not falling under the Clinical Trials Regulations)
- An Introduction to GCP
- Legislation
- Protocol and Associated Documents
- Documentation and Study Files
- Applications, Approvals and Amendments
- Confidentiality
- Consent and conducting the study
- Web Resources
| Course Name | Date | Time |
|---|---|---|
| GCP for Clinical Research Studies | 28-Oct-13 | 9 am - 3.30 pm (full) |
How to Book
Please contact karl.shepherd@admin.ox.ac.uk or tel. 01865 572221 if you would like to attend any of the above courses.
Note: To enable us to provide training free of charge, we regret that we are not able to provide lunch or refreshments.