Site Monitoring. Develop and Implement monitoring plan E Conduct monitoring (Source document verification, drug accountability, regulatory document review, eCRF review, supply inventory, etc.) E Identify and report non-compliance E Provide written monitoring reports E Conduct Site close-out procedure (final source document verification, drug accountability, regulatory document review, eCRF review, study supply disposition, etc.) E
Appears in 2 contracts
Sources: Clinical Trial Agreement (Nugenerex Immuno-Oncology, Inc.), Clinical Trial Agreement (Generex Biotechnology Corp)
Site Monitoring. A. Develop and Implement monitoring plan E E
B. Conduct monitoring (Source document verification, drug accountability, regulatory document review, eCRF review, supply inventory, etc.) E E
C. Identify and report non-compliance E E
D. Provide written monitoring reports E E
E. Conduct Site close-out procedure (final source document verification, drug accountability, regulatory document review, eCRF review, study supply disposition, etc.) E
Appears in 1 contract