TASC SOPs and templates: Study start up

TASC has developed a library of SOPs and templates for the study start up category

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SOP 14 - Writing a Protocol to Good Clinical Practice for Clinical Trials of Investigational Medicinal Products

SOP 18 - Trial Set Up in Clinical Trials of Investigational Medicinal Products

SOP 19 - Preparing and Maintaining Case Report Forms (CRF) for use in Clinical Research

SOP 23 - Completion of Delegation Log

SOP 28 - Sponsorship of Clinical Trials

SOP 29 - Application for Sponsorship of Health and Social Care Research Studies (excluding Drug (e.g. CTIMP) and Device Studies)

SOP 45 - Establishing and Maintaining a Trial Master File, Investigator Site File and Pharmacy Site File for use in Clinical Research 

SOP 47 - The use of Version Control of Study Documents used in Health and Social Care Research Studies

SOP 54 - Training Records

SOP 61 - Registering and Reporting Research in a Publicly Accessible Database

SOP 64 - Risk Assessment of Clinical Research on Behalf of the Sponsor

‌SOP 66 - Planning Patient and Public Involvement (PPI) In Clinical Research

SOP 67 - Advanced Therapy and Gene Modification Safety Committee Approval For Clinical Research