The Trusted Standard in Research, Ethics, Compliance, and Safety Training

The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners.

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Celebrating 24 Years of Serving Education and Science Communities
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Utilized by the Top-25 Ranked U.S. Hospitals
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Over 15 Million Learners with 25+ Million Course Completions
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Utilized by the Top-25 Best National Universities*
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95% of Carnegie R1 Research Universities are 10+ year subscribers


Explore Our Featured Courses

Controlled Unclassified Information Controlled Unclassified Information
New

Understand CUI and the obligations it creates for universities and researchers.

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Service Dogs in Science: Barriers to Inclusion Service Dogs in Science: Barriers to Inclusion
New

A systematic approach to exploring the barriers, steps, methods, and solutions for including service dog handlers in science.

samson the service dog in the lab
Operationalizing and Incorporating Telehealth Operationalizing and Incorporating Telehealth
Featured

This series is ideal for organizations looking to establish and incorporate telehealth in healthcare and education settings.

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Fraud, Waste, and Abuse Fraud, Waste, and Abuse
Featured

Learn about fraud, waste, and abuse (FWA) and ways to prevent and report FWA.

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Research Security Research Security
Featured

These courses explore key topics related to research security and international engagement.

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Medical Residents and Fellows: Basic Principles of Research Medical Residents and Fellows: Basic Principles of Research
Featured

Foundational overview of clinical research meant to prepare medical residents and fellows to conduct their own research and work on research teams.

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The Role of Data Managers in Clinical Trials The Role of Data Managers in Clinical Trials
New

The webinar details the functions of clinical data managers in the production of clinical trial results.

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OHRP: Participant-Centered Informed Consent Training OHRP: Participant-Centered Informed Consent Training
New

Learn how to create participant-centered informed consent forms through this interactive training.

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Promoting Healthy Authorship Dynamics in Research Teams Promoting Healthy Authorship Dynamics in Research Teams
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Explores the role institutions can play in supporting ethical authorship practices and resolving authorship disputes.

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The Importance of Mentorship in Biomedical and Behavioral Research The Importance of Mentorship in Biomedical and Behavioral Research
FeaturedNew

Examines mentorship in biomedical and behavioral research, which is critical to advancing science.

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Emerging Technologies and Homeland Security Emerging Technologies and Homeland Security
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Explores the challenges and opportunities emerging technologies present to homeland security, covering topics such as cyber threats, ransomware, drone misuse, IoT vulnerabilities, AI threats, disinformation, and deepfakes.

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The Importance of Mentorship in Biomedical and Behavioral Research The Importance of Mentorship in Biomedical and Behavioral Research
FeaturedNew

Examines mentorship in biomedical and behavioral research, which is critical to advancing science.

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Why AI Companies Should Care About Ethics Why AI Companies Should Care About Ethics
Featured

Explores the importance of ethics for AI companies and its impact on public trust and profitability.

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RCR and Grant Stewardship RCR and Grant Stewardship
New

Learn how grant stewardship obligations are a part of responsible conduct of research.

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Space Exploration: The Future of Human Subject Research Ethics Space Exploration: The Future of Human Subject Research Ethics
Featured

Explores ethical and regulatory considerations for human subjects research in outer space.

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Bystander Intervention Training Bystander Intervention Training
Featured

Empower yourself to effectively intervene and support others in critical situations with our comprehensive Bystander Training course.

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Emergency Preparedness and Response for HRPPs Emergency Preparedness and Response for HRPPs
New

Explores considerations for a human research protection program (HRPP) emergency preparedness plan.

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Field Research Safety: Assessing and Managing Risk Field Research Safety: Assessing and Managing Risk
FeaturedNew

A systematic approach to preparing for and adjusting to risks associated with wilderness field research.

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Infection Control/Prevention and Pandemics Infection Control/Prevention and Pandemics
Featured

A review of infection prevention, lessons learned, and preparing for future pathogens.

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Title IX – Faculty and Staff Title IX – Faculty and Staff
Featured

An in depth look at the federal Title IX law and required compliance of faculty, staff, and administrators.

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Utilizing Outside Experts on the IRB Utilizing Outside Experts on the IRB
Featured

Explores what is known about IRB utilization of outsize expertise.

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CRA Relationships with CRCs CRA Relationships with CRCs
Featured

Details ways to produce productive partnerships between clinical research associates and clinical research coordinators.

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Peer Review Fundamentals Peer Review Fundamentals
Featured

Covers the purpose, best practices, and emerging models for peer review.

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Sustainable Science: How to Make Research Labs Greener Sustainable Science: How to Make Research Labs Greener
Featured

Discusses the environmental impact of research in the U.S., how to mitigate the environmental impact of research operations, and ways to involve key stakeholders in mitigating the environmental impact of research operations.

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Essentials of Statistical Analysis (EOSA) Essentials of Statistical Analysis (EOSA)
New

Covers the essentials of statistical analysis to help learners gain greater statistical literacy.

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Biotility: Good Documentation Practices (GDP) Biotility: Good Documentation Practices (GDP)
Featured

Strategies for implementing compliance with GDP, as well as standards and procedures for accurately completing Records required for current cGMP.

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Biotility: Regulatory Approval for Medical Devices (United States) Biotility: Regulatory Approval for Medical Devices (United States)
Featured

Describes FDA’s regulatory controls for common marketing approval pathways for the classes of medical devices, and explains the Code of Federal Regulations that pertain to medical device approval in the U.S.

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The Network of Networks (N2) The Network of Networks (N2)
Featured

N2 is a not-for-profit alliance of Canadian research networks and organizations working to enhance national clinical research capability and capacity.

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BIC Study Foundation BIC Study Foundation
Featured

BIC Study Foundation is a resource for those who want to take CITI Program courses in Korean. They are a certified training provider by the Korean FDA/MAFRA for HRPP and ACU Programs.

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OneAegis OneAegis
Featured

A complete research compliance suite that supports IRB, IACUC Conflict of interest, Bio Safety Export Control, and more.

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HRP Consulting Group – Research Consulting Services HRP Consulting Group – Research Consulting Services
Featured

HRP Consulting provides customized services for your research program, including temporary staffing, IRB/IACUC assistance, accreditation support, program evaluations, training/education and more.

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CTrials by BRANY CTrials by BRANY
Featured

CTrials helps grow sponsored research programs by taking on the many administrative challenges inherent in managing clinical trials.

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Informed Consent Builder Informed Consent Builder
Featured

Informed Consent Builder is a cloud-based platform that streamlines the process of managing and generating informed consent forms.

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Protocol Builder Protocol Builder
Featured

Protocol Builder is an online protocol writing and collaboration platform that also speed up your pre-review turnaround times.

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Join Over 2,500 Subscribing Organizations

Highlighted below are just a few select subscribers & collaborators.

Meet A Few Of Our Expert Authors and Presenters

Our courses are built by over 350 highly qualified experts and rigorously peer reviewed to incorporate various perspectives and ensure accuracy, completeness, and overall quality.

content contributor emily dacquisto

Emily Dacquisto, MSW

University of Maryland

Emily Dacquisto is a Faculty Assistant and Program Manager in the University of Maryland’s College of Information Studies. Her current research projects include big data and data ethics, privacy policy, content moderation, and values-centered AI. She holds an MSW from the University of Minnesota and a BA from the University of Iowa.

content contributor dessi kirilova

Dessi Kirilova, MA

Qualitative Data Repository

Dessi Kirilova is the senior curation specialist at the Qualitative Data Repository (QDR). In addition to assisting researchers planning to publish their social science data, she teaches and publishes on topics around research transparency, data curation and the ethics of data sharing, including the role of IRBs.

content contributor kira dunn

Kira Dunn, CISSP, CRISC, PMP

University of California San Diego

Kira Dunn has 13 years of cybersecurity experience in the higher education and healthcare industries, encompassing technical writing, project management, risk assessment, and compliance gap analysis. She is currently a Senior Risk and Compliance Analyst, focusing on Cybersecurity Maturity Model Certification (CMMC) compliance for the University of California’s oceanic research.

Content Contributor Linda Reuter

Linda Reuter, MS, CIP

Biomedical Research Alliance of New York (BRANY)

Linda has been involved with IRB Administration in various capacities over a 30-year period, currently serving as the Sr. Director for BRANY IRB. Linda also formed IRB Consulting, LLC in 2012, providing IRB administrative services, training and education, audit services, and general consulting to numerous IRB programs across the country.

In Our Learners' Words

tony p

Tony P.

English Language Arts Teacher

I liked how user-friendly the course modules were.

armando t

Armando T.

Adjunct Faculty

The methodology, presentation of the topics, and language used were very pleasant. You do not get bored or annoyed, because the development is very dynamic and understandable.

tiina m

Tiina M.

PhD Student

The course was short and well divided into sub-themes that were easy to understand and retain.

johanna s

Johanna S.

Manager, Research Operations

The knowledge checks while reviewing information assisted with retention and provided clarifications with examples of real-world application.

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Courses Approved by Top Continuing Education Accreditors

CITI Program courses are approved for CME credits through the Albert Einstein Montefiore Continuing Professional Development Center (CPDC). Albert Einstein College of Medicine-Montefiore Medical Center (Einstein) is accredited by the Joint Accreditation for Interprofessional Continuing Education to provide continuing education activities for healthcare professionals. Einstein is accredited to offer continuing education credit for the following professions: medicine, nursing, psychology, pharmacy, dentistry, optometry, social work, nutritional science, and athletic training.

CITI Program is also accredited by the International Accreditors for Continuing Education and Training (IACET) and offers IACET CEUs for its learning events that comply with the ANSI/IACET Continuing Education and Training Standard. IACET is recognized internationally as a standard development organization and accrediting body that promotes quality of continuing education and training.

View CE Certified Courses

Recent News & Articles

New Webinar: Controlled Unclassified Information – What it is, Isn’t, and University Obligations
Content Update News

New Webinar: Controlled Unclassified Information – What it is, Isn’t, and University Obligations

This webinar provides a better understanding of 32 CFR Part 2002, including the safeguarding requirements.

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What CITI Program is Reading – October 9, 2024
Blog

What CITI Program is Reading – October 9, 2024

“What CITI Program is Reading” is our biweekly blog series which highlights news articles curated by our staff and relevant to research, higher education, healthcare,...

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Free Live Webinar – A Recovering IRB Chair’s Guidance to Students Who Want to Do Research
Upcoming Events

Free Live Webinar – A Recovering IRB Chair’s Guidance to Students Who Want to Do Research

This webinar offers some practical advice from a recovering IRB Chair for students who want to do research.

Read the article