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
This course provides graduate students with practical guidance, strategies, and resources to confidently navigate each stage of the dissertation process from proposal to defense.
Provides learners with an examination of developments in ICH Good Clinical Practice.
Describes how to build a fit-for-purpose regulatory strategy that strengthens your business strategy and differentiates your product in today’s digital health market.
The course provides fundamental knowledge of the principles and practices of clinical research.
The RCR Casebook course is a collection of real-world ethical dilemmas designed to promote discussion, critical thinking, and skill-building in RCR.
Provides a foundational overview of quantitative methods, equipping learners with the essential tools to analyze and interpret numerical data for research and decision-making.
Provides hands-on knowledge of reception and scheduling best practices.
Provides an overview of research security requirements and researcher responsibilities and best practices.
An introductory video-based series to the DOE’s SBIR-STTR funding program and a discussion of key elements of the proposal elements.
Foundational overview of clinical research meant to prepare medical residents and fellows to conduct their own research and work on research teams.
Introduces you to key information about, and tools to use, the 3Rs of animal research.
Covers the regulatory aspects related to SaMD and CDSS when conducting clinical investigations and other considerations.
Prepares you to apply digital health ethics in healthcare and research.
Provides an introduction to the EU AI Act, including risk-based approaches, compliance obligations, enforcement, interplays with other European digital policy, and perspectives
Provides an in-depth review of the elements of informed consent.
This course provides learners with a review of contemporary bioethics issues.
This webinar reflects on the creation of a culture of compliance through the lens of how one university created an enterprise-wide compliance role.
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.
An overview of Medicare for healthcare operations, covering Parts A, B, C, and D as well as key aspects of its administration, audits, and oversight.
A review of HIPAA’s HITECH Act of 2009 geared toward business associates, vendors, and others subject to HIPAA.
Provides learners with emerging concepts and practices for creating research facilities.
Explains how the Common Rule applies to secondary research with data and biospecimens.
Discusses regulations and emergency response considerations for colleges and universities with research reactors, nuclear chemistry programs, and linear accelerators.
An introduction to risk management and crisis response within study abroad programs.
Discusses how to adopt a virtual first care (V1C) approach in your work.
Designed to provide information on how to adopt and integrate telehealth technologies into the delivery of the National Diabetes Prevention Program.
Covers different categories of replacements, considerations for various personnel, and references for further learning.
Discusses the four pillars of a culture of care, the impact of compassion fatigue, and individual and institutional strategies to address compassion fatigue.
Provides an overview of the current trends and incorporation of automation and digitalization in research vivariums.
Stress at research institutions is common, explore ways to navigate and mitigate the effects of stress in these settings.
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. Moin Syed is a McKnight Presidential Endowed Professor in the Department of Psychology at the University of Minnesota. He has conducted numerous workshops on methods, open science, preregistration, diversity, and theory development across the U.S. and Europe, and has been heavily involved in science reform efforts.
Dr. Pallant is the Clinical Director of Health Services at Brown University in Providence, RI. He completed his pediatric residency and chief residency at UCSF in California, and his MD and PhD in Immunology and Microbiology at the University of Rochester School of Medicine and Dentistry.
Dr. Blackman-Siddall is a licensed clinical psychologist and retired USAF officer. Currently, she serves as the Research Protections Program Manager at Capella University. She manages the IRB and the Research Compliance team, and she investigates alleged academic integrity violations and research misconduct in advanced doctoral projects.
Diana Kapiszewski is Provost's Distinguished Associate Professor of Government at Georgetown University as well as Senior Research Associate with the Qualitative Data Repository. Her research focuses on research methods, transparency, and ethics; as well as comparative politics. She has published widely on techniques for generating and sharing qualitative data.
In Our Learners' Words
Althea S.
PhD Student
The modules about the laws that explain protected populations were very informative. I also appreciated the section on safeguards put in place to protect subjects participating in studies.
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.
Tony P.
English Language Arts Teacher
I liked how user-friendly the course modules were.
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.
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 Course – Working with Birds in Research Settings
This course discusses research mandates, basic care and handling, biological features and behavioral characteristics, occupational health hazards and more.
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What CITI Program is Reading – July 17, 2025
“What CITI Program is Reading” is our biweekly blog series which highlights news articles curated by our staff and relevant to research, higher education, healthcare,...
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Free Live Webinar – Being Creative when Applying the IRB Exemptions: Part 1
This presentation will discuss the concept of IRB exemptions and the role they play in regulated and unregulated research.
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