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Clinical Research Resource HUB

tools, templates, guidance and go-to ...

The HUB provides a single portal to resources, expertise, and best practices for investigators, study staff, participants and partners/affiliates.

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Who You Are

  • Investigators
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Trial Management

  • Budgeting & Billing
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  • Data Management
  • Feasibility & Scientific Review
  • Protocol Development
  • Recruitment Strategy
  • Regulatory Binder
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  • Study Management

Regulatory

  • 21 CFR Part 11 Compliance
  • ClinicalTrials.Gov
  • FDA & OHRP Inspections
  • FDA Alerts
  • IDE Development Process
  • IND Development Process
  • SOPs

Training

  • APex / STOR / UCare
  • Clinical Trial Budgeting
  • Good Clinical Practice
  • Human Subjects
  • iMedRIS / CHR
  • Investigator Resources
  • OnCore
  • Research Coordinator
  • Safety Courses

UCSF Quick Reference

  • Contracts & Grants
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  • Ethics & Compliance
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  • ICH GCP Guidelines
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  • MyAccess
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About the HUB

  • Contact Us
  • HUB Vision & Goals
  • Who We Are
  • Cancer Center
  • Clinical & Translational Science Institute
  • Contracts & Grants
  • Core Search
  • CTSI Clinical Research Services
  • Environmental Health & Safety
  • Global Health Research
  • Human Research Protection Program
  • Industry Contracts

The HUB is a collaborative effort of the Office of Research, the Office of Ethics and Compliance and the Clinical & Translational Science Institute (CTSI).

Not finding what you need?     Contact Us      |      HUB@ucsf.edu      |      415.476.9371      |      415.476.9429

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