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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Utilized by the Top-25 Ranked U.S. Hospitals
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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

Introduction to Healthcare Compliance Introduction to Healthcare Compliance
New

This course introduces the essentials of healthcare compliance, including key fraud and abuse laws, Medicare billing, HIPAA, risk assessment, auditing, and the core elements of an effective compliance program.

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Principal Investigator’s Guide to ClinicalTrials.gov Principal Investigator’s Guide to ClinicalTrials.gov
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Practical guidance for investigators on ClinicalTrials.gov registration, results reporting, review criteria, and ongoing compliance.

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Intellectual Property for Students and Postdocs Intellectual Property for Students and Postdocs
New

IP for Students and Postdocs introduces early-career researchers to intellectual property fundamentals, helping them identify, protect, and responsibly share innovations from academic and research settings.

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IRB Review of Expedited Research IRB Review of Expedited Research
New

This course covers expedited categories, helping IRB members and administrators identify minimal-risk studies, apply appropriate regulations, and make clear, consistent decisions.

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Biotility: Lead Document Controller Biotility: Lead Document Controller
New

Introduces document control principles, Good Documentation Practices, and responsibilities of lead document controllers.

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Data Privacy 101 Data Privacy 101
Featured

Provides essential training on why privacy awareness and compliance matter.

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3Rs Certificate Course 3Rs Certificate Course
Featured

Introduces you to key information about, and tools to use, the 3Rs of animal research.

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NIH SBIR-STTR Funding NIH SBIR-STTR Funding
Featured

Covers the NIH SBIR-STTR proposal process, from program eligibility and proposal development to submission, award implementation, and business-university partnerships.

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Research Ethics for All (RE4All) Research Ethics for All (RE4All)
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Provides community research partners with disability-accessible education on ethical issues in social and behavioral research.

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Community Research Partner Training Community Research Partner Training
Featured

This course equips community partners with the knowledge and skills to ethically and effectively engage in research.

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Establishing a Clinical Research Program Establishing a Clinical Research Program
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Provides instructions for creating the structures, personnel, and funding for a clinical research program.

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Regulation of Food‑Producing Animals Used in Research Regulation of Food‑Producing Animals Used in Research
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Covers the ethical, regulatory, and practical considerations for using food‑producing animals in research, including veterinary oversight, biosecurity, regulated drug use, and food safety compliance.

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Software Development Ethics Software Development Ethics
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A comprehensive introduction to ethical principles, regulations, and responsible practices that guide software and technology professionals throughout the software development lifecycle.

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Bioethics Bioethics
CME/CEUFeatured

This course provides learners with a review of contemporary bioethics issues.

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Ethical Research Relationships: IRBs and Focus Groups Ethical Research Relationships: IRBs and Focus Groups
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This webinar covers ethical focus group practices, including informed consent, confidentiality, and Institutional and Tribal IRB oversight.

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Being Creative when Applying the IRB Exemptions: Part 1 Being Creative when Applying the IRB Exemptions: Part 1
Featured

Examines the application of IRB exemptions, focusing on overlooked flexibilities in categories 1 through 3 through discussion and real-world examples.

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Redefining Ethical Research Practice in the Age of AI Redefining Ethical Research Practice in the Age of AI
Featured

Explores the transformative impact of AI on biomedical research, addressing its unique characteristics, potential to exacerbate health disparities, and the urgent need to redesign research processes and incentives to ensure ethical and equitable knowledge discovery.

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The Essential Guide to Forming a Research Integrity Standing Committee The Essential Guide to Forming a Research Integrity Standing Committee
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This webinar examines the key considerations, structures, and practical steps for forming a successful Research Integrity Standing Committee.

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Diagnosis Coding: Using the ICD-10-CM Diagnosis Coding: Using the ICD-10-CM
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This course offers practical training on ICD-10-CM structure, coding conventions, and official guidelines to support accurate diagnosis coding, proper billing, and audit readiness across leadership roles.

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Artificial Intelligence and the Medicare Coverage Analysis Artificial Intelligence and the Medicare Coverage Analysis
New

This webinar outlines key requirements, exceptions, and compliance steps under the NIH Policy on Enhancing Security Measures for Human Biospecimens.

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NIH Biospecimens Rule NIH Biospecimens Rule
New

This webinar outlines key requirements, exceptions, and compliance steps under the NIH Policy on Enhancing Security Measures for Human Biospecimens.

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Applying AI in GMP Auditing: Current Practices and Future Perspectives Applying AI in GMP Auditing: Current Practices and Future Perspectives
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Explains how AI can be responsibly integrated into GMP auditing to enhance audit execution, data integrity, and compliance while anticipating emerging regulatory and risk considerations.

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Seven Elements of an Effective Compliance Program: What Research Administrators Need to Know Seven Elements of an Effective Compliance Program: What Research Administrators Need to Know
Featured

This webinar for IRB, IACUC, and sponsored program administrators covers seven key compliance elements with strategies and case studies to strengthen research, reduce risk, and promote integrity.

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Radiation Safety Radiation Safety
Featured

A detailed review of radiation safety for research and medical institutions.

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Research Integrity for Senior and Key Personnel Research Integrity for Senior and Key Personnel
Featured

This course offers advanced training for experienced researchers and leaders in responsible research conduct, emphasizing integrity, ethical leadership, and fostering healthy research environments.

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Advanced Mentorship Training Advanced Mentorship Training
Featured

Equips research personnel with the skills and insights necessary for effective mentorship.

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Quantitative Research: What IRBs Need to Know Quantitative Research: What IRBs Need to Know
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Explains why and how IRBs must assess quantitative research design as an ethical issue, including risks like poor methodology, participant burden, data privacy, and AI-generated data contamination.

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Becoming an Effective Leader Becoming an Effective Leader
CME/CEUFeatured

Helps develop leadership skills to meet today’s changing, diverse, and dynamic environments.

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Crosstalk Between the IACUC and IBC Crosstalk Between the IACUC and IBC
Featured

The webinar explores effective collaboration between IACUC and IBC, detailing their roles, regulatory responsibilities, and best practices to ensure safe and ethical life sciences research while enhancing oversight and protecting workers and animals.

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Regulatory Landscape and Practical Challenges in Cellular Therapy Regulatory Landscape and Practical Challenges in Cellular Therapy
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Describes the development, regulatory framework, and safety considerations for HCT/Ps.

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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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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

Join Over 3,000 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 jefferey botkin

Jeffrey Botkin, MD, MPH

University of Utah

Dr. Botkin is a Professor of Pediatrics at the University of Utah, Adjunct Professor of Human Genetics and Adjunct Professor of Internal Medicine. He is the former Associate Vice President for Research Integrity at the University and has held national positions including as member and Chair of SACHRP.

content contributor giovanni de gregorio

Giovanni De Gregorio, PhD

Universidade Católica Portuguesa

Giovanni is an Associate Professor in Law and Technology at Católica Global School of Law.

content contributor dennis shung

Dennis L. Shung, MD, MHS, PhD

Yale School of Medicine

Dennis L. Shung, MD, MHS, PhD, is an Assistant Professor of Medicine at Yale School of Medicine and Director of Digital Health in Digestive Diseases. He leads the Human+Artificial Intelligence in Medicine lab, which focuses on enhancing human presence with AI. Shung is also involved in multiple gastroenterology AI initiatives and research.

blanca guillen woods bio

Blanca Guillen-Woods, MA

SLP4i

Blanca Flor Guillén-Woods, Partner at SLP4i, has implemented several applied research and evaluation projects, including multi-site and multi-year projects working with disenfranchised communities. Her experience includes research design, fieldwork, public opinion polling, conducting focus groups, facilitating community meetings, and quantitative and qualitative data analyses.

In Our Learners' Words

shamsul q

Shamsul Q.

Head of Department of Pathology/Microbiology

Excellent course. I enjoyed it fully and increased my level of knowledge in specific scenarios.

gowramma ip

Gowramma I.P.

Professor of Education

The detailed content and clarity, with examples and case studies, are what I liked best. The ability to switch between reading and A/V modes when required was also useful.

william h

William H.

Human Resources Intern

I like how the quiz results elaborate greatly on the nuances and anything noteworthy that contributes to understanding the logic behind the answer, not just knowing the answer.

tiina m

Tiina M.

PhD Student

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

Recent News & Articles

New Course – Introduction to Healthcare Compliance
Content Update News

New Course – Introduction to Healthcare Compliance

This course provides a comprehensive overview of the essential principles and regulatory requirements for building and maintaining effective compliance programs.

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On Research Podcast – Beyond Persistence: How Early-Career Scientists Can Thrive
Blog

On Research Podcast – Beyond Persistence: How Early-Career Scientists Can Thrive

Season 3 – Episode 18 – Beyond Persistence: How Early-Career Scientists Can Thrive In this episode, we discuss what it takes for early-career scientists to...

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Synthetic Biology and Cancer: Progress and Promise Webinar Series
Upcoming Events

Synthetic Biology and Cancer: Progress and Promise Webinar Series

This webinar series will highlight technical advances, translational insights, and future directions in synthetic biology and cancer research.

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