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
A comprehensive introduction to ethical principles, regulations, and responsible practices that guide software and technology professionals throughout the software development lifecycle.
Provides community research partners with disability-accessible education on ethical issues in social and behavioral research.
Provides instructions for creating the structures, personnel, and funding for a clinical research program.
Provides learners with an understanding of the principles of inventory management.
The course explores OPSEC in academia, training faculty, staff, and students to identify and mitigate risks to sensitive research data while upholding open science principles.
An introductory video-based series to the U.S. Department of War/U.S. Department of Defense SBIR-STTR funding program and a discussion of key elements of the proposal and proposal process.
Serves as research security training designed to augment RECR/RCR training.
Introduces you to key information about, and tools to use, the 3Rs of animal research.
Equips research personnel with the skills and insights necessary for effective mentorship.
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.
The IRB Review of Exempt Research course provides an overview of the exempt categories of research per 45 CFR 46.104 and discusses considerations for making an exempt determination per regulatory criteria.
This course provides learners with a review of contemporary bioethics issues.
The RCR Casebook course is a collection of real-world ethical dilemmas designed to promote discussion, critical thinking, and skill-building in RCR.
Explore the impact of academic integrity from the perspective of both students and faculty/staff.
Prepares you to apply digital health ethics in healthcare and research.
Practical information on the fundamentals of being a Principal Investigator (PI).
This course provides training on working with birds in research settings.
This webinar explains the DOJ Bulk Data Transfer Rule, its key requirements, and how data mapping supports compliance with NIH biospecimen security expectations.
This series provides a comprehensive overview of cybersecurity in healthcare, exploring organizational strategies, technical defenses, and risk management practices to safeguard data, operations, and trust.
Equips university faculty, staff, administrators, and students with essential knowledge on Title IX compliance and program assessment to foster safer, more effective, and student-centered campus environments.
Describes the regulatory framework and quality programs for HCT/Ps
Provides learners with an understanding of environmental regulations affecting the biotech industry.
The synergistic relationship between best practices, regulations, and professional experience forms the foundation for working in a BSL-3 facility.
Helps clinical and operations leaders move from AI exploration to confident, ethical, and effective implementation.
Helps develop leadership skills to meet today’s changing, diverse, and dynamic environments.
Explores practical, ethical, and regulatory strategies for designing and reviewing research involving younger populations, emphasizing risk mitigation, regulatory flexibility, and effective collaboration between researchers and IRBs.
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.
Explores the benefits and the considerations of working with consultants on research misconduct investigations.
Provides an overview of conflict, types of conflict, conflict styles, communication styles, and intervention strategies.
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.
Dr. Dumsha has been at Philadelphia College of Osteopathic Medicine since 1995. Her office is responsible for administering the IRB and IACUC. Jane has been a member of the American Medical Writers Association since 1981 and a Certified Health Education Specialist since 1997. She earned her PhD from Trident University.
Assistant Vice Chancellor for Regulatory Affairs, IRB Executive Chair, and Professor of Pediatrics, University of Nebraska Medical Center. AAHRPP Council on Accreditation; previously Board of Directors, PRIMR; co-editor of the 3rd edition of “IRB: Management and Function”, author of numerous papers, chapters, review articles regarding ethics and human subject protections
Danielle Louder serves as Co-Director of MCD Global Health’s U.S. Programs and Director of the Northeast Telehealth Resource Center. In these roles she is responsible for growth of the U.S. based portfolio in alignment with MCD’s mission, and advancing use of digital health strategies to improve health access and outcomes.
Richard Paul is a licensed MD with extensive experience in drug development, drug safety, global regulatory affairs, and translational clinical research. He has held leadership positions in clinical research, regulatory and medical safety departments with pharmaceutical companies. His experience spans medical safety, medical monitoring, drug development, and regulatory strategy.
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.
Maria E.
Evidence Based Practice Nursing Resident, Diabetes Nurse Specialist
Great information on the importance of protections in research with human subjects. I liked the audiovisual option.
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.
El Pagnier H.
Senior Vice President, Human Resources/Doctoral Student
The course had excellent content that was clearly presented.
Recent News & Articles
New Course – Intellectual Property for Students and Postdocs
Foundational course designed for graduate students, postdoctoral scholars, and early‑career researchers working in academic or research environments.
Read the article
What Are the Fair Information Practice Principles (FIPPs)? A Privacy Guide
Overview In an era when data is often called the “new oil,” most of us feel a lingering unease about how our personal information is...
Read the article
MeRTEC Three I’s Biosecurity And Research Integrity
Join the NESBR, MeRTEC, and NCABR, for the 2026 Three I’s Conference focused on promoting responsible conduct and ethics in research.
Read the article