Posts

• Updated! UUSOP-02 FDA
• New! UUSOP-06-A Supplement
• Updated! UUSOP-13: Fee Schedule
• Updated! UUSOP-13 A Supplement
• Did you know...UUSOP-05: Delegation of Authority
• Did you know...UUSOP-06: Study Records Management
• Did you know…UUSOP-08: Obtaining Written Informed Consent

• Updated! UUSOP-05: Delegation of Authority
• New! UUSOP-07-A Supplement
• Updated! UUSOP-09: Case Report Form Completion Standards
• Updated! UUSOP-11: Investigational New Drug Applications in FDA Regulated Research
• Updated! UUSOP-12: Investigational Device Exemption Applications in FDA Regulated Research
• Updated! UUSOP-13: Fee Schedule
• Updated! UUSOP-13 A Supplement
• Updated! UUSOP-14: Clinical Trial Safety Assessment and Reporting
• New! UUSOP-16: FORM FDA 1572

• Updated! UUSOP-02: FDA Inspections
• New! UUSOP-02-A Supplement
• New! UUSOP-08-A Supplement
• Updated! UUSOP-05: Delegation of Authority
• Updated! UUSOP-11: Investigational New Drug Applications in FDA Regulated Research
• Updated! UUSOP-12: Investigational Device Exemption Applications in FDA Regulated Research
• Updated! UUSOP-13: Fee Schedule
• Updated! UUSOP-13 A Supplement
• New! UUSOP-15: Internal Monitoring of University of Utah Clinical Studies

• Updated! UUSOP-02: FDA Inspections
• Updated! UUSOP-06: Study Records Management
• Updated! UUSOP-06-A: Study Records Management, Supplement A
• Updated! UUSOP-07: Deviations: Documentation and Reporting
• Updated! UUSOP-10: Monitoring Visits for Externally Sponsored Clinical Trials
• Updated! UUSOP-13: Institutional Fee Schedule and UUSOP-13-A: Fee Schedule Cost Rationale
• New! FAQ on Source vs. Worksheets vs. CRFs

An updated version of UUSOP-07: Deviations - Documentation and Reporting will be released in December 2023 for immediate implementation. The FDA has recently been observed to issue 483 letters to investigators that have deviated from the IRE-approved protocol with what is referred to as "sponsor approval."...