Research and Development Policies
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- Safety Reporting in Clinical Research Policy (pdf, 450 KB)
- See templates for Serious Adverse Events Reporting Form and related templates, below
- Sponsorship of Clinical Research Studies (pdf, 346 KB)
- Capacity and Capability Approval for Clinical Research (pdf, 336 KB)
- Monitoring and Audit of Clinical Research Studies (pdf, 337 KB)
- Research Passports, Honorary Research Contracts and Letters of Access Policy (pdf, 349 KB)
- Integrity in Clinical Research Policy and Procedure (pdf, 292 KB)
- Research Access to Notes Registration Form (Word, 48 KB)
- Intellectual Property Policy (pdf, 264 KB)
Templates for Standard Operating Procedures (SOPs)
- Archiving of Essential Documents (Word, 59 KB)
- Case Report Form Completion (Word, 57 KB)
- Clinical Device Protocol Template (Word, 228 KB)
- Clinical Research Study Protocol Template (Word, 81 KB)
- Clinical Trial Protocol Template (Word, 103 KB)
- Database Design (Using Excel) (Word, 2.8 MB)
- Design and Development of Case Report Forms (Word, 77 KB)
- Document Control (Word, 62 KB)
- Ethics Committee Application (Word, 69 KB)
- Feasibility Questionnaire (Word, 516 KB)
- Informed Consent (Word, 74 KB)
- Preparation and Approval of Protocol Amendments (Word, 65 KB)
- Qualitative Research Study Protocol Template (Word, 54 KB)
- Template for creating Standard Operating Procedures (Word, 53 KB)
