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 & Billing
Data Safety Monitoring
Data Management
Feasibility Guidance
Protocol Development
Recruiting Strategy
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
Good Clinical Practice
Human Subjects
iRIS / IRB Submissions
Investigator Education
OnCore
Safety Courses
Glossaries
You are here
Home
>
Resources for...
>
Study Staff
Resources for Study Staff
Pre-Study
Informed Consent Development
Coordinator Training
Good Clinical Practice
iRIS / IRB Submissions
Recruitment Strategy
Pre-Study Budgeting
Study Set-Up
Cancer Research Activation Workflow (USA and international studies)
Regulatory
21 CFR Part 11 Compliance
Clinical Trials.Gov
Data & Safety Monitoring
IND Development
IDE Development
Regulatory Binder
SOPs
Study Management
Data Management
Research Billing
Specimen Management
New!
Clinical Labs Research Specimen Transportation Service
Study Management
Subject Enrollment
Quality Management