ResearchGo | UCLA Skip to main content Investigator Support Services Main CTSI Homepage Search ResearchGO COVID-19 Info Explore by RoleInvestigators & FacultyStudy StaffParticipantsPartners & 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 ResearchGO provides a single portal to resources, expertise, and best practices for investigators, study staff, and partners/affiliates Design Study Set Up Study Conduct Study Close Out Study Recently Updated Resources DSMPs and DSMBs at UCLA August 10, 2026 DSMPs and DSMBs at UCLA The UCLA Human Research Protection Program requires an adequate data and safety monitoring plan (DSMP) for all interventional research studies involving greater-than-minimal... Data and Safety Monitoring August 10, 2026 Data & Safety Monitoring  The NIH requires data and safety monitoring for all types of clinical trials, including physiologic, toxicity, and dose-finding studies (phase I); efficacy studies (... Data Management Guidance July 24, 2026 Data Management Guidance Data management plans (DMPs) encourage researchers to think about how they will responsibly handle the data they collect, and are required by many funders. The National... CTSI Partners Can’t find what you need? Contact ResearchGo Group 1Clinical Research Information Systems UCLA Clinical Trials Group 2Office of Research Administration Jonsson Comprehensive Cancer Center Group 3Office of Human Subjects Protection CareConnect Website © 2022 The Regents of the University of California. All rights reserved.