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  1. Tools
  2. Templates & Resources

Templates & Resources

Note: Some links may require logging in with your AD credentials.

  • Clinical Study Management Process
  • Creating Study Design
  • Glossary of Lay Terms for Use in Preparing Protocols for the IRB
  • ICH Essential Documents for the Conduct of a Clinical Trial
  • IRB Assurance Letter/FWA Letter 
  • Personal Vehicle Usage for UCSD Business (see Blink page for Insurance Requirements and Liability Issues)
  • Protocol Overview Fact Sheet Template 
  • Quick Reference Guide - Clinical Trial and Investigator-Initiated Agreements 
  • Radiation Risk Calculator
  • Registration of Clinical Trials in a Public Registry for Publication
  • Research Acronyms & Definitions
  • Storage Facilities
  • Velos: UCSD's Clinical Trial Management System
  • Sample Standard Operating Procedure
  • Standard Operating Procedure Template
  • Regulatory Binder Template
Last updated: 17 Sep 2019
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    • EPIC Electronic Medical Record | EMR
    • Research Charge Reconciliation
  • Regulatory Maintenance
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    • Research Compliance and Integrity Office
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    • Mandatory Reporting | ClinicalTrials.gov
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    • Research Account | Velos (coming soon)
  • Clinical Research Billing | CRB
  • Human Research Protections Program | HRPP
  • Office of Coverage Analysis Administration | OCAA
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  • Investigational Drug Service | IDS
  • Office of Research Affairs | ORA
  • Environmental Health & Safety | EH&S
  • Office of Clinical Trials Administration | OCTA
  • Health Sciences Office of Compliance & Privacy | OCP
  • HS Sponsored Project Pre-Award Office | HSSPPO
  • UC Learning Center | UCLC
  • Altman Clinical & Translational Research Institute | ACTRI

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