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5) Trial Operation (T)

T1 Study start up

T2 Approach and Identification of Participants for Research

T3 Consent procedures for entry into a Research study

T4 Case Report Form (CRF) completion

T5 Safety reporting

T6  Non-compliance reporting

T7 Urgent Safety Measures

T8 Research Study Amendments

T9 Periodic Reports to REC & MHRA

T10 Recording of study data

T11 Provision of virology test information

T12 Researcher Audit Guidance Jan 2019

T13 Consistency of images for clinical research

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