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
Introduces a systematic method for analyzing safety statistics
An introductory video-based series to the DOE’s SBIR-STTR funding program and a discussion of key elements of the proposal elements.
This course explores explores technological advances and eConsults.
Introduces you to key information about, and tools to use, the 3Rs of animal research.
These courses explore key topics related to research security and international engagement.
Provides learners with best practices for creating and maintaining study documents.
Covers how to identify red flags in your survey data, strategies to develop surveys to minimize fraud, and best practices for data management.
Understand CUI and the obligations it creates for universities and researchers.
Explores considerations for a human research protection program (HRPP) emergency preparedness plan.
Learn how to review nonexempt human subjects research protocols for regulatory compliance with the Common Rule.
Provides learners with key information on the management of controlled substances in clinical research settings.
This role-based course provides the practical know-how to monitor clinical research sites effectively.
Provides an introduction to the EU AI Act, including risk-based approaches, compliance obligations, enforcement, interplays with other European digital policy, and perspectives
An introduction for students to the meaning of academic integrity and plagiarism.
Explores common motives behind fraudulent survey research participation, how to address and mitigate the impact of identified fraudulent data, and how to minimize opportunities for malicious intent.
Explores strategies for remaining diligent about securing online survey research.
Examines ethical and policy issues about xenotransplantation.
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.
This webinar reflects on the creation of a culture of compliance through the lens of how one university created an enterprise-wide compliance role.
Discusses what events must reported, to whom, and according to what timeline.
Learn about the FCPA and its impact to healthcare operations.
This webinar offers practical solutions for optimizing corporate board roles to foster a culture of ethics and compliance.
A role-based course that provides practical know-how to effectively lead or participate on data monitoring committees.
Overview of the European Union’s (EU) General Data Protection Regulation (GDPR).
Discusses the four pillars of a culture of care, the impact of compassion fatigue, and individual and institutional strategies to address compassion fatigue.
The webinar explores work-related musculoskeletal disorders among surgical teams.
An introduction to risk management and crisis response within study abroad programs.
An in-depth review of advanced topics important to research administrators.
Stress at research institutions is common, explore ways to navigate and mitigate the effects of stress in these settings.
This course focuses on promoting the success of international students on university campuses by offering strategies for academic support, cultural integration, and compliance with U.S. federal policies.
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.
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.
Dr. Shelley Victor is Professor Emeritus at Nova Southeastern University. She teaches courses in Supervision, Ethics, and Professional Issues. She became ASHA Fellow in 2000 and received Honors of Florida Association of Speech-Language Pathologists and Audiologists in 2002. She has presented and published on the topic of supervision since 1995
Cheryl has over 30 years of high level experience in biomedical and SBR research administration, coupled with 15 years in research compliance consulting, recently founding Savini Consulting LLC. Her expertise spans across both national and international research, serving as an IRB member and personal experience as a research subject.
Robert Michalik is an FDA regulatory attorney and founder of RegulatoryPro Consulting, which serves biopharmaceutical and medical device clients. He has law and biochemistry degrees and has worked for over 30 years in the biopharmaceutical and medical device industries. He counsels clients in technical, quality, and regulatory areas related to new product development and commercialization activities.
Iris Palmer is deputy director for community colleges with the Education Policy program at New America. She is a member of the higher education team and the Center on Education & Labor. She provides research and analysis on community colleges and the ethical use of predictive analytics in higher education.
In Our Learners' Words
William J.
Cluster Director of Pharmacy & Research
The interactive modules are amazing. It’s like being at a course in person, but with the ability to review something if extra help is needed.
Xianjie Q.
Biostatistics Graduate Student
I like how there are two different view modes for the modules, there are explanations after every quiz question, and I can retake the quiz.
James B.
Medical Doctor, Health Coach
I liked how the material was posted with big words, spaced, and simple English. The adverse drug event and monitoring sections were very informative.
Hailey G.
Research Assistant - Undergraduate Student
The course was very informative and provided a great elaboration on the concepts discussed. I found it important to incorporate the historical aspect of the research field and how it has evolved over time. The case studies allowed for a constructive self-evaluation of the material within each module. The videos were also a productive form of reinforcing the concepts discussed.
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.
Recent News & Articles
New Webinar – FDA IND Safety Reporting for Clinical Trial Investigations
Study sites and sponsors are responsible for reporting AEs, SAEs, ADRs, SUSARs, UPs, and UADEs according to detailed instructions of FDA guidances.
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CITI Program Funding Finds – April 16, 2025
“CITI Program Funding Finds” is our monthly blog series which highlights opportunities relevant to research grants, funding, programs open to new applicants, and more. Follow...
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Free Live Webinar – ARRIVE Guidelines for Reporting Animal Research
This webinar addresses the critical issue of reproducibility in preclinical research.
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