SOPs for management, in-progress, and close down of sponsored clinical trials of medicinal products

SOP for the classification, review and submission of clinical trial amendments

SOP for the Recording and Reporting of Deviations, Violations, Potential Serious breaches, Serious breaches and Urgent Safety Measures

SOP for Archiving Essential Documents relating to CTIMPs

SOP for the Preparation and Submission of Development Safety Update Reports

SOP for Preparation and Maintenance of the Trial Master File (TMF)/ Investigator Site File (ISF) for CTIMPs Sponsored by UCL

SOP for Investigators and Sponsor for End of Trial Notification and Trial Close Out Procedures