Skip to main content
University of California San Francisco
UCSF Health
Search UCSF
About UCSF
Clinical Research Resource HUB
Search form
Search...
Resources for...
Investigators
Study Staff
Participants
Partners / Affiliates
Study Design
Study Set-Up
Study Conduct
Study Close-Out
Trial Management
Consent Development
Coverage Analysis
Data Safety Monitoring
Data Management
Feasibility Guidance
Protocol Development
Recruitment Resources
Regulatory Binder
Safety Reporting
Study Management
Regulatory
21 CFR Part 11 Compliance
ClinicalTrials.gov
FDA & OHRP Inspections
FDA Alerts
IDE Development Process
IND Development Process
SOPs
Clinical Laboratory Testing
Training
APeX / STOR & other
Clinical Research Coordinators
Human Subjects
iRIS / IRB Submissions
Investigator Education
OnCore
Safety Courses
Glossaries
You are here
Home
>
Resources for...
>
Investigators
Resources for Investigators
Last revised
:
04/24/2024
Pre-Study
Conflict of Interest
Consent Development
Funding Opportunities
iRIS / IRB
Investigator Resources
Protocol Development
Feasibility & Review
Trial Budgeting
Cancer Research Activation Workflow (USA and international studies)
Innovation Ventures
Work with Community
Center for Community Engagement
Regulatory
ClinicalTrials.Gov
Data & Safety Monitoring
IDE Development
IND Development
Regulatory Binder
Site Inspections
Study Management
Data Management
Good Clinical Practice
Quality Management
Budgeting & Billing
APeX
UCSF Care Everywhere and Research Policy for Clinical Research Coordinators
Specimen Management
Clinical Labs Research Specimen Transportation Service
Study Management Tools
SOPs