Research and development
Documentation - Standard Operating Procedures and Policies
All Studies
- SOP-01-08 SOP on SOPs
- SOP-04-07 Informed Consent
- SOP-06-07 TMF
- SOP-07-06 Research Staff Training
- SOP-09-08 Amendments
- SOP-17-05 Archiving Essential Documents
- SOP-19-06 QMS
- SOP-21-05 Trial Closure
- SOP-22-06 End of Trial Study Reports
- SOP-35-02 Exiting Staff Procedure
Trust Sponsored Studies
- SOP-02-09 SAEs (Sponsored)
- SOP-08-05 Role of CI, Pharmacy, Nuclear Medicine and R&D
- SOP-10-05 Serious Breaches (Sponsored)
- SOP-11-05 Sponsor Oversight
- SOP-12-04 Monitoring
- SOP-13-05 Research Applications
- SOP-14-05 Writing Research Protocols
- SOP-15-06 CRF and Data Management (Sponsored)
- SOP-16-07 DSURs
- SOP-18-06 Initiation
- SOP-20-06 Patient Information
- SOP-28-06 Source Data
- SOP-32-06 Vendor Assessment
- SOP-33-04 Risk Assessment Process
- SOP-34-02 Statistics
Hosted Studies
For staff
SOP Signature Sheet – once all SOP have been read this signature sheet should be completed, signed and obtained in Staff training file
Policies
The documents on this page are PDFs. To view them you will need Adobe Acrobat Reader.
Click this image to download the latest version of Adobe Reader
Documents for Download
- Costing Pro-forma - Microsoft Word document opens in a separate applicaion
- Patient Information Documents - Microsoft Word document opens in a separate applicaion
- Model Agreements - Opens in a new window
- Template CV - Microsoft Word document opens in a separate applicaion