Research and Development SOPs are listed below for your information.
- S01 – Preparation of SOPs in R&D
- S02 – Submitting Protocol Amendments
- S03 – Archiving
- 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 – Confirmation of Capacity and Capability
- S22 – Safety Reporting
- S23 – Conduct of Home Visits
- S26 – Training for Researchers
- S29 – Letter of Access Research Passport
- S31 – Reporting for sponsored CTIMPs
- S32 – Screening Patients
- S36 – Spinning and Storage of Blood Samples
- S39 – Venepuncture in Infants and Children
- S42 – Storage and Transportation of Clinical Samples
- S43 – Establishing a TMF ISF
- S45 – Transportation temperature sensitive CT meds
- S47 – Clinical trial participant pregnancy
- S48 – Non-CTIMP Sponsorship
- S51 – Unblinding Subjects Emergency
- S52 – Urgent Safety Measures
- S60 – Electronic Transfer of Prescriptions to Trial Pharmacy
- S63 – Urgent Public Health Research
- S64 – Data Capture and Cleansing
- S65 – Randomisation
- S66 – Managing Emergencies outside Main Template