Skip to main content
Investigator Support Services
Main CTSI Homepage
Search ResearchGO
COVID-19 Info
Explore by Role
Investigators & Faculty
Study Staff
Participants
Partners & Affiliates
Go
Search form
Search
Toggle navigation
Stages of Research
Design Study
Set Up Study
Conduct Study
Close Out Study
Clinical Study Management
Ancillary Research Services
Consent Development
Contracts & Grants
Coverage Analysis
Data & Safety Monitoring
Data Management
Feasibility and Scientific Review
Protocol Development
Quality Management
Recruitment Strategy
Regulatory Binder
Research Billing
Research Pricing
Safety Reporting
Study Management
UCLA Trial Innovation Network
Regulatory
21 CFR Part 11 Validation
ClinicalTrials.Gov
FDA Inspections & Alerts
IDE Development Process
IND Development Process
IRB Process / IBC Process
SOPs
Training
CareConnect/Research Connect
Clinical Research Coordinators
Good Clinical Practice
Human Subjects / IRB Process
OnCore
Safety Courses
UCLA Investigators
OCR Links
Clinical Research Finance
Clinical Trials Contracts & Strategic Relations
Coordination Services & Education
Embedded Clinical Research & Innovation
FDA Affairs
Office of Regulatory Affairs
Research Quality & Navigation
CTSI Links
CTSI CTRCs
Clinical Data Requests
Community Engagement
Integrating Special Populations
NIH Clinical Trials and Human Subjects
Partners & Affiliates
Research Cores
Home
Send by email
Send by email
Your email
*
Your name
Send to
*
Subject
*
Page to be sent
Integrating Special Populations (ISP)
Your message
*
Send email
Cancel
