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
These courses explore key topics related to research security and international engagement.
A foundational course that teaches researchers to fully integrate qualitative and quantitative approaches for rigorous, ethical, high-quality mixed methods research.
Equips research personnel with the skills and insights necessary for effective mentorship.
This course offers advanced training for experienced researchers and leaders in responsible research conduct, emphasizing integrity, ethical leadership, and fostering healthy research environments.
This course prepares researchers and educational technology developers to navigate COPPA’s legal requirements, conduct compliant research, and engage with digital environments used by children under 13.
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.
An introductory video-based series to the NSF’s SBIR-STTR funding program and a discussion of key elements of the proposal and proposal process.
This course provides training on working with insects in research settings.
Covers various considerations for reviewing human subjects research, including subject selection, risk minimization, balancing risks and benefits, and privacy and confidentiality.
Provides hands-on knowledge of research accounting principles and practices.
Introduces you to key information about, and tools to use, the 3Rs of animal research.
Prepares you to apply digital health ethics in healthcare and research.
Covers the principles, governance approaches, practices, and tools for responsible artificial intelligence (AI) development and use.
Explores how behavioral science can enhance compliance programs.
This course provides foundational training on conflicts of interest for healthcare professionals.
Provides learners with an understanding of environmental regulations affecting the biotech industry.
Provides learners with best practices for maintaining document control in a research setting.
Explores underutilized IRB exemptions and highlights flexible approaches, especially in categories 4 through 8, through discussion and real-world examples.
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.
Explores how researchers and IRB reviewers can collaborate to navigate the complexities of research involving youth.
An in depth look at the federal Title IX law and required compliance of faculty, staff, and administrators.
This course equips faculty, staff, and administrators with the fundamentals and tools to measure outcomes, improve learning, and effectiveness.
Provide your organization's learners with access to currently available and future webinar recordings.
Provides a foundational overview of quantitative methods, equipping learners with the essential tools to analyze and interpret numerical data for research and decision-making.
An overview of PCTs, their ethical complexities, best practices, and institutional considerations.
Provides instruction on how to improve your teaching and training skills in a variety of settings.
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 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.
Tom is a globally recognized leader in education research, policy, and entrepreneurship. He teaches education entrepreneurship and consulting at NYU and runs his own consulting firm. Tom has built a track record of creating strategic partnerships with policy makers, researchers, practitioners and corporations.
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.
Donna Evans is a clinical research manager at Moffitt Cancer Center in Tampa, FL where she oversees Radiation Oncology, Bone Marrow Transplant and Immunotherapy Research Departments. Over a 15 year career in research she has worked as a coordinator, administrator, and director. Evans graduated with her MS from George Washington University.
Knowledgeable research professional with over 15 years of experience in academic animal research.
In Our Learners' Words
Emma M.
Student
This was one of the best courses I have taken due to the easy reading and watching of videos that prepare you for the quizzes.
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.
Timothy F.
PhD Candidate
The course was very informative and detailed. I also appreciated the case studies to assist in understanding how these concepts are applicable.
Juliana S.
Medical Student
The reading material was simple, concise, but also very informative in regards to the most important points.
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