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.
These courses explore key topics related to research security and international engagement.
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 research personnel with the skills and insights necessary for effective mentorship.
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.
Describes the regulatory framework and quality programs for HCT/Ps
This interactive course helps university students understand their Title IX rights and responsibilities, including how to recognize, prevent, and report sexual misconduct and discrimination.
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 equips community partners with the knowledge and skills to ethically and effectively engage in research.
This course provides essential practices for those working with high-risk biological materials, clarifying biosafety vs. biosecurity and enabling practical biosecurity planning to prevent theft, misuse, or intentional release.
This course equips faculty, staff, and administrators with the fundamentals and tools to measure outcomes, improve learning, and effectiveness.
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.
Examines the application of IRB exemptions, focusing on overlooked flexibilities in categories 1 through 3 through discussion and real-world examples.
Introduces you to key information about, and tools to use, the 3Rs of animal research.
The RCR Casebook course is a collection of real-world ethical dilemmas designed to promote discussion, critical thinking, and skill-building in RCR.
Covers the principles, governance approaches, practices, and tools for responsible artificial intelligence (AI) development and use.
Explores how behavioral science can enhance compliance programs.
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.
Explores how generative AI (GenAI) can support science communication.
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.
Explores issues that lead to research misconduct and ways to develop trust with faculty and leadership.
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.
Reviews two of the foundational elements of the Common Rule—when something is or is not research and when an individual is or is not a human subject.
Provides an in-depth review of the elements of informed consent.
A detailed review of the IRB meeting and membership requirements.
This course provides graduate students with practical guidance, strategies, and resources to confidently navigate each stage of the dissertation process from proposal to defense.
Provide your organization's learners with access to currently available and future webinar recordings.
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.
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.
Describes how to calculate the appropriate sample size for different study designs and outcomes.
Explores the benefits and the considerations of working with consultants on research misconduct investigations.
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.
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.
Highlighted below are just a few select subscribers & collaborators.
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.
Bill Hinchcliffe serves as Radiation Safety Officer and Assistant Radiation Safety Officer for Bridgeport Hospital and Yale New Haven Hospital (YNHH), respectively. He has both his BS and MS in Health Physics from Purdue University and Idaho State University. Bill has been serving in his role at YNHH since 2010.
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
As the Head of Digital Scholarship at Boston College, Sarah led a group that teaches technical topics. Her team facilitated data-driven research, project creation, and digital publishing. Now Sarah consults on topics related to digital scholarship, such as open access publishing. Sarah received her PhD from Emory University in 2017.
Dr. Celi is the principal investigator behind the Medical Information Mart for Intensive Care and its offspring, MIMIC-CXR, MIMIC-ED, MIMIC-ECHO, and MIMIC-ECG. With close to 100k users worldwide, an open codebase, and close to 10k publications in Google Scholar, the datasets have shaped the course of machine learning in healthcare.
Clinical Nurse Specialist and Instructor
Very user-friendly
Clinical researcher
As a researcher with very little prior training in the regulatory aspects of research conduct, the information in this module was very helpful.
Professor
The course touches on important research considerations in a manageable format. The material required that I pay attention but did not tax my concentration.
Senior Vice President, Human Resources/Doctoral Student
The course had excellent content that was clearly presented.
New Course – Operations Security in Academia
Explores OPSEC in academia, training faculty, staff, and students to identify and mitigate risks to sensitive research data while upholding open science principles.
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Clinical Decision Support Compliance: FDA’s 2026 Expectations
Overview On January 6, 2026, the FDA issued an updated final guidance, “Clinical Decision Support Software: Guidance for Industry and Food and Drug Administration Staff,”...
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Federal Demonstration Partnership January 2026 Meeting
Join The Federal Demonstration Partnership (FDP) for its virtual meeting on January 26-28, 2026.
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