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Regulatory Affairs
ClinicalTrials.gov Registration
Good Tissue Practice
ORRA Monitoring Unit
Study Monitoring
Study Management Tools
Adverse Event Log (Device)
Adverse Event Log (Drug)
Compensation Log
Concomitant Medication Log
Delegation of Authority Log
Deviation Log
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Eligibility Checklist
IND – IDE Monitoring Plan
Informed Consent Process Note
Regulatory Binder Contents
Role of the Medical Monitor
Screening-Enrollment Log
SIV Agenda
Source Data Agreement
Specimen Tracking Log
ORRA Regulatory Unit
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Investigational New Drug Submission
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University of Arkansas for Medical Sciences
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