Standard Operating Procedures (SOPs)
Chief and Principal Investigators, all other research personnel who have been delegated roles and responsibilities and the staff of the R&D Department who have the function of research governance for our hospitals must adhere to this set of procedures when undertaking research.
- SOP 01 Preparation of SOPs
- SOP 02 Research Documentation and File Management
- SOP 03 Training
- SOP 04 Informed Consent in Research
- SOP 05 End of Trial Procedures
- SOP 06 Trial Archiving
- SOP 07 Managing Participant Expenses
- SOP 08 - Unblinding Treatments
- SOP 09 Medicines Management
- SOP 10 Hosting CTIMPs and other Clinical Studies
- SOP 11 Confirmation of Capacity and Capability
- SOP 13 – Monitoring and Oversight of Hosted Studies
- SOP 14 - Study Income Distribution
- SOP 15 Research Studies Involving Sue Ryder
- SOP 16 Managing MHRA Inspection
- SOP 17 Radiotherapy trial management at satellite sites
- SOP 18 Application Process for an Honorary Contract, Letter of Access or Research Passport
- SOP 19 Periodic Safety Reporting
- SOP 20 Adverse events and reaction safety reporting
- SOP 23 Urgent Safety Measures
- SOP 24 Scientific Peer Review
- SOP 25 Staff Surveys
- SOP 29 Writing a protocol
- SOP 30 Workplace Visitors
- SOP 31 PA Allocation Process
- SOP 32 Change of PI
- SOP 33 – Due Diligence
- SOP 35 - Electronic health records document Sharing with sponsors
- SOP 37 – Process for submitting Expression of Interest for Academic Studies
- SOP 38 - Monitoring and oversight of sponsored studies