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Research and Innovation: Office of Research Regulatory Affairs
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          • Adverse Event Log (Device)
          • Adverse Event Log (Drug)
          • Compensation Log
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          • IND – IDE Monitoring Plan
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  1. University of Arkansas for Medical Sciences
  2. Research and Innovation
  3. Office of Research Regulatory Affairs
  4. Departments
  5. Regulatory Affairs
  6. Monitoring Unit
  7. Study Management Tools

Study Management Tools

Local Resources

  • Regulatory Binder Contents
  • Sample Site Initiation Visit Agenda
  • Sample Monitoring Plan
  • Financial Disclosure Form
  • Sample Adverse Event Log (Device)
  • Sample Adverse Event Log (Drug)
  • Sample Concomitant Medication Log
  • Sample Compensation Log
  • Sample Delegation of Authority Log
  • Sample Device Accountability Log (Use)
  • Sample Device Accountability Log (Receipt-Return-Repair-Destruction)
  • Sample Deviation Log
  • Sample Eligibility Checklist
  • Sample Informed Consent Process Note
  • Sample Screening-Enrollment Log
  • Sample Source Data Agreement
  • Sample Specimen Tracking Log
  • Device Risk Determination Checklist
  • Role of the Medical Monitor

Subpages

  • Adverse Event Log (Device)
  • Adverse Event Log (Drug)
  • Compensation Log
  • Concomitant Medication Log
  • Delegation of Authority Log
  • Deviation Log
  • Device Accountability Log
  • Device Accountability Log (Use)
  • 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
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Mailing Address: 4301 West Markham Street, Little Rock, AR 72205
Phone: (501) 686-7000
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