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SOPs for Ïã¸ÛÁùºÏ²Ê sponsored CTIMPs

SOPs and guidance relevant to CI’s for ATIMPs, CTIMPs and medical device studies which are sponsored by Ïã¸ÛÁùºÏ²Ê and managed through the JRO (only).

SOP for granting Ïã¸ÛÁùºÏ²Ê sponsorshipÌý

SOP for the preparation and maintenance of the TMF and ISFÌý(Updated 5 August 2024)

SOP for obtaining REC, CTA & HRA for CTIMPs

SOP for creating and maintaining anÌýIBÌý

SOP for preparation for randomisation blinding and code breaksÌý(Updated 13 August 2024)

SOP on training for staff Ìýparticipating in CTIMPs Sponsored by Ïã¸ÛÁùºÏ²Ê

SOP for the Recording, Management and Reporting of Adverse Events by InvestigatorsSOP for the oversight and monitoring of Ïã¸ÛÁùºÏ²Ê sponsored CTIMPs

SOP for Recording and Reporting of Deviations, Violations, Serious Breaches and Urgent Safety MeasureÌý[updated 3 July 2024]

SOP for the classification, review and submission of AmendmentsÌý(Updated 5 August 2024)

SOP on DSUR

SOP for End of Trial NotificationÌý

SOP for ArchivingÌý

SOP for Electronic SignatureÌý

Protocol templates for Ïã¸ÛÁùºÏ²ÊÌýsponsored research

  • Ïã¸ÛÁùºÏ²Ê CTIMP protocol template (provided by JRO Clinical Trials team as part of sponsorship submission)

  • Ïã¸ÛÁùºÏ²Ê Advanced therapy trials protocol template (provided by JRO ATIMPs team as part of sponsorship submission)

Lab index and feasibility questionnaire templates

Templates for supporting documents

The package of supporting documents you will need to provide will depend on the type of application and the type of research activity that is planned. Supporting documents include:

SOP for Peer Review for studies sponsored by Ïã¸ÛÁùºÏ²ÊÌý(Last updated 11/12/2023)Ìý

Standard Operating Procedure for JRO Administration of Research PassportsÌý(Last updated 11/12/2023)

Ïã¸ÛÁùºÏ²Ê Complaints from Research Subjects About Ïã¸ÛÁùºÏ²Ê Sponsored StudiesÌýand TrialsÌýpolicy