Clinical Research Toolkit

This toolkit of materials contains templates, sample forms and information materials to assist clinical investigators in the development and conduct of high-quality clinical research studies. All files on this page link directly to a Word file maintained on the NIH website unless otherwise noted. Need assistance? Contact Regulatory Specialist Sheila Austin, 352-273-8702.

Regulatory Binder Checklist (NIH)

The following 12 items can be found in this checklist from the National Institutes of Health, which downloads as a Word document.

  • Delegation of Responsibilities Log
  • Documenting the Consent Process
  • Financial Disclosure Form (see page 40)
  • Investigational Product Accountability Drug –  Stock Record Log
  • Investigational Product Accountability Device – Stock and Subject Log (Word document downloaded from NIH May 2019 and maintained on this site)
  • Monitoring Visit Log
  • Protocol Deviation Tracking Log
  • Regulatory Document Log – List of all documents submitted to the FDA
  • Site Screening and Enrollment Log
  • Specimen Tracking Log
  • Subject Code Log – NIH (Word document downloaded from NIH May 2019 and maintained on this site)
  • Training Log

Subject File Tools (NIH)

  • Informed Consent Process Checklist Subject
  • Investigational Product Accountability Drug –  Subject Record Log

Miscellaneous File Tools

Quality Management Tools (NIH)

UF Institutional Review Board Tools

SOPs