Skip to main content
  • Investigator Support Services
  • Main CTSI Homepage
  • Search ResearchGO
  • COVID-19 Info
Home

Search form

  • Stages of Research
    • Design Study
    • Set Up Study
    • Conduct Study
    • Close Out Study
  • Clinical Study Management
    • Billing, Coding & Pricing
    • Budgeting
    • Consent Development
    • Contracts & Grants
    • Coverage Analysis
    • Data & Safety Monitoring
    • Data Management
    • Feasibility and Scientific Review
    • Protocol Development
    • Quality Management
    • Recruitment Strategy
    • Regulatory Binder
    • 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
    • Ancillary Research Services
    • CareConnect/Research Connect
    • Clinical Research Coordinators
    • Good Clinical Practice
    • Human Subjects / IRB Process
    • OnCore
    • Safety Courses
    • UCLA Investigators
  • CTSI Links
    • CTSI CTRCs
    • CTSI Regulatory Affairs
    • Clinical Data Requests
    • Community Engagement
    • Coordination Services & Education
    • Embedded Clinical Research (ECRI)
    • Integrating Special Populations
    • NIH Human Subjects Updates
    • Research Cores
  • CTSI Partners
    • Cedars-Sinai
    • Charles R. Drew University
    • Lundquist/Harbor-UCLA
  1. Home
  2. Stages of Research
  3. Conduct Study

Conduct Study

Study Management

Clinical Research Billing

Coverage Analysis & Budget Information

Billing, Coding & Pricing

Oncore - CRMS

CareConnect Research

Biostatistics

HIPAA

Specimen Management

Standard Operating Procedures (SOPs)

Requesting Help with Enrollment, Ethics & more

Access Electronic Health Records

Request a Consultation - Ethics (Bedside)

Request a Consultation - Ethics (Benchside)

Participant Recruitment

Review Regulatory & Compliance Resources and References

Regulatory Support and Services

Medical Center Policies 

Review Regulatory Binder Requirements

FDA Inspections/Audits

Responsible Conduct of Research

Data Sharing

Records Management & Information Practices

 

  • Printer-friendly version
  • Send by email
  • PDF version

Last updated: 29 Nov 2022

Can’t find what you need?

Contact ResearchGo
310-794-8969

  • Group 1
    • Clinical Research Information Systems
    • Clinical Research Business Partners
  • Group 2
    • Office of Research Administration
    • Jonsson Comprehensive Cancer Center
  • Group 3
    • Office of Human Subjects Protection
    • CareConnect Website

© 2022 The Regents of the University of California. All rights reserved.