Research and Development SOPs are listed below for your information.

• S01 – Preparation of SOPs in Research and Development
• S02 – Submitting Protocol Amendments
• S03 – Archiving     
• S04 – Auditing Processes
• S05 – Serious Breaches of Good Clinical Practice or Trial Protocol
• S06 – Scientific Review
• S07 – Contracts
• S08 – Costing Non-Commercial Network Studies
• S09 – CTIMP Sponsorship
• S11 – Delegation of Roles
• S13 – Regulatory Approvals
• S14 – Honorary Contracts
• S15 – Informed Consent
• S19 – Monitoring
• S21 – Applying for Trust Approval
• S22 – Safety Reporting
• S23 – Conduct of Home Visits
• S24 – Study Specific SOPs
• S26 – Training for Researchers
• S29 – Research Passport SOP
• S31 – Reporting for sponsored CTIMPs
• S32 – Screening Patients
• S36 – Spinning and Storage of Blood Samples
• S39 – Venepuncture in Infants and Small Children
• S40 – Risk Assessment
• S42 – Storage and Transportation of Clinical Samples
• S43 – Establishing a TMF ISF
• S45 – Transportation of Vaccines
• S46 – Decontamination of Clinical Trial Biological Sample Spillage
• S47 – Clinical Trial Participants and Pregnancy
• S48 – Non CTIMP Sponsorship
• S51 – Unblinding Subjects Emergency
• S52 – Urgent Safety Measures
• S60 – Prescription transfer
• S63 – Urgent Public Health Research
• S64 – Data Capture and Cleansing
• S65 – Randomisation
• S66 – Managing Emergencies outside Main Template