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.
Explore Our Featured Courses
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.
These courses explore key topics related to research security and international engagement.
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.
Introduces document control principles, Good Documentation Practices, and responsibilities of lead document controllers.
A comprehensive introduction to ethical principles, regulations, and responsible practices that guide software and technology professionals throughout the software development lifecycle.
Provides instructions for creating the structures, personnel, and funding for a clinical research program.
Provides community research partners with disability-accessible education on ethical issues in social and behavioral research.
This webinar explores how researchers can use GenAI to strengthen research design, from refining questions and methods to improving data plans and addressing ethical considerations.
Serves as research security training designed to augment RECR/RCR training.
Provides essential training on why privacy awareness and compliance matter.
This course equips community partners with the knowledge and skills to ethically and effectively engage in research.
Introduces you to key information about, and tools to use, the 3Rs of animal research.
Provides an overview of participatory science and the associated ethical and IRB review challenges.
Introduces you to key information about, and tools to use, the 3Rs of animal research.
This webinar covers ethical focus group practices, including informed consent, confidentiality, and Institutional and Tribal IRB oversight.
Examines the application of IRB exemptions, focusing on overlooked flexibilities in categories 1 through 3 through discussion and real-world examples.
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.
An introductory webinar for new RIOs as they start their journey.
Explains how the Common Rule applies to secondary research with data and biospecimens.
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.
Provides learners with an understanding of the principles of inventory management.
This webinar explains the DOJ Bulk Data Transfer Rule, its key requirements, and how data mapping supports compliance with NIH biospecimen security expectations.
Provides a review of what COI committee members need to know.
Describes the regulatory framework and quality programs for HCT/Ps
The synergistic relationship between best practices, regulations, and professional experience forms the foundation for working in a BSL-3 facility.
Explores how generative AI (GenAI) can support science communication.
Describes how to calculate the appropriate sample size for different study designs and outcomes.
Presents a scalable model for creating a research coordinator float pool to provide flexible staffing, structured training, and broad support for clinical research across institutions.
Provides an overview of conflict, types of conflict, conflict styles, communication styles, and intervention strategies.
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.
Helps clinical and operations leaders move from AI exploration to confident, ethical, and effective implementation.
N2 is a not-for-profit alliance of Canadian research networks and organizations working to enhance national clinical research capability and capacity.
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.
A complete research compliance suite that supports IRB, IACUC Conflict of interest, Bio Safety Export Control, and more.
HRP Consulting provides customized services for your research program, including temporary staffing, IRB/IACUC assistance, accreditation support, program evaluations, training/education and more.
CTrials helps grow sponsored research programs by taking on the many administrative challenges inherent in managing clinical trials.
Informed Consent Builder is a cloud-based platform that streamlines the process of managing and generating informed consent forms.
Protocol Builder is an online protocol writing and collaboration platform that also speed up your pre-review turnaround times.
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.
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.
Megan Gunn, MD MAUB, is an Assistant Professor of Clinical Medicine in the Division of General Internal Medicine and Public Health at Vanderbilt University Medical Center.
Amanda Kraus serves as Assistant VP for Campus Life and Executive Director for Disability Resources at the University of Arizona. UA’s Disability Resource Center is considered an international model of progressive service delivery. She is also Associate Professor of Practice in Higher Education where she teaches courses on student services and disability. Dr. Kraus travels the country and abroad to give talks on ableism and universal design.
Dr. Werbinski, an ObGyn and Clinical Associate Professor Emerita at WMed, teaches sex-specific medicine there. Past President of AMWA, and co-founder of its Sex and Gender Women’s Health Collaborative, she advocates for fundamental change in women’s healthcare, considering the ways in which women’s and men’s risks, treatments, and outcomes differ.
Nick Ciancio is the sustainability coordinator at the University of Alabama at Birmingham. Nick has worked at UAB since 2015, where he started the green labs program. Nick currently works to reduce electricity consumption, waste generation, and water usage across research buildings campus-wide.
In Our Learners' Words
Julie S.
Assistant Professor & Postdoctoral Research Fellow
These courses were easy to access and succinct, which made a review of the Belmont Report key tenets, as well as the review of differences between practice and research, a focused and time efficient endeavor.
Jon F.
Former Bioethics Teacher & Current Ethics Committee Member
I liked the high level and detail of the course material. I found it to be challenging, but when I finished the course, I felt a real sense of accomplishment.
Shamsul Q.
Head of Department of Pathology/Microbiology
Excellent course. I enjoyed it fully and increased my level of knowledge in specific scenarios.
Molly O’R.
Graduate Student
The course had clear and concise explanations, was visually appealing, and the audio was helpful for comprehension. The speed and clarity of audio was great.
Recent News & Articles
New Course – Principal Investigator’s Guide to ClinicalTrials.gov
The course provides step‑by‑step guidance on navigating the PRS, managing records, responding to review feedback, and maintaining compliance throughout a study’s lifecycle.
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FDA Warns 2,200 Sponsors: Are You Compliant with ClinicalTrials.gov?
Overview On April 13, 2026, the U.S. Food and Drug Administration (FDA) reminded over 2,200 clinical trial sponsors and researchers of their legal duty to...
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Fueling Cancer Progression by the Nervous System Webinar – Cancer Neu...
This webinar will focus on the cancer neuroscience of brain metastasis.
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