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Content Topics

Academic Integrity – Student

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Accident Investigation: An Introduction

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ADA, Accessibility, and Accommodations in Higher Education

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All Access Webinar Package (Organizations Only)

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Animal Care and Use (ACU) Core

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Animal Care and Use (ACU) Advanced

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Becoming an Effective Leader

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Big Data and Data Science Research Ethics

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Bioethics

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Biomedical Principal Investigator

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Biosafety and Biosecurity (BSS)

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Biosafety Level 3 (BSL-3) Practices and Procedures

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Biotility @UF

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Campus Health and Wellness

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Clery Act Training

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Clinical Research: An Introduction

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Clinical Research Coordinator (CRC)

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Clinical Trial Billing Compliance (CTBC)

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Compensation Reporting (Effort Reporting)

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Conflict Management

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Conflicts of Interest and Commitment

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Controlled Substances in Research Settings

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Data Management for SBE Research

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Data Monitoring Committees: A Guide for New Leaders and Members

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Disaster Planning and Response

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Essentials of Clinical Trial Budgets

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Essentials of Grant Proposal Development

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Essentials of Pharmacovigilance

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Essentials of Research Administration

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Essentials of Responsible AI

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Essentials of Statistical Analysis (EOSA)

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Export Compliance (EC)

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False Claims Act: A Primer and Guide for Research Organizations

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Federal Fraud and Abuse Laws

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FMLA in Higher Education

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FDA Inspections: From Site Preparation to Response

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Foreign Corrupt Practices Act (FCPA)

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GDPR for Research and Higher Ed

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General Laboratory Safety for Non-Laboratory Personnel

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Good Clinical Practice (GCP)

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Good Laboratory Practice (GLP)

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Good Manufacturing Practices (GMP)

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Health Insurance Portability and Accountability Act (HIPAA)

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Healthcare Ethics Committee (HEC)

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Human Subjects Research (HSR)

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Infection Prevention in Healthcare Settings

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Information Privacy & Security (IPS)

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Institutional Review Board (IRB) Administration

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IRB Protocol Review

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Introduction to Equity and Diversity in Clinical Research and Trials Participation

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Laboratory Chemical Safety

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Laboratory Decontamination Methods

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Laser Safety

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Medical Monitoring for Drugs and Biologics

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Navigating Online and Hybrid Teaching

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Medical Residents and Fellows: Basic Principles of Research

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Observational Research Protocols: An Introduction

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Preparing for Success in Scholarly Publishing

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Protocol Development and Execution: Beyond a Concept

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Protocol Registration & Results Disclosure in ClinicalTrials.gov

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QA/QI: Human Subjects Research

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Qualitative Data Analysis

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Radiation Safety

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Research Security

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Research Study Design

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Responsible Conduct of Research (RCR)

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Responsible Conduct of Research (RCR) Facilitator Guides

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SBIR/STTR Grants and Compliance

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Science Fairs: Essentials for Educators and Participants

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Survey Research: Design, Planning, Implementation, and Ethics

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Teaching and Training for Professionals

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Technology, Ethics, and Regulations

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Technology Transfer

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Title IX – Faculty and Staff

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Workplace Ergonomics

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Customize Your CITI Program

Customize Your CITI Program

CITI Program can be adapted to meet specific organizational, language, country, or discipline needs. For instance, your organization can select content from across CITI Program courses included in your subscription and add institutional-specific content. You can also request customized instructions, contact information, and reporting. In addition, we may be able to translate content into languages that are not already provided for an additional fee.

Plus, we offer services such as Single-Sign-On, which enables learners to log in to CITI Program with the same user name and password they use for your organization’s information systems. We can discuss your specific needs after you subscribe or you can contact us to learn more now.