Continuing Education Unit Ceu Credit for Completed Citi Program Courses

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.

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Over 10 Million Learners with 19+ Million Course Completions

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Utilized by the Top-25 Ranked U.S. Hospitals

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Celebrating 22 Years of Serving Education and Science Communities

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95% of Carnegie R1 Research Universities are 10+ year subscribers

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Utilized by the Top-25 Best National Universities*

Explore Our Featured Courses

QA/QI: Human Subjects Research

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Learn about QA/QI programs, how to conduct an internal audit, and strategies for using the findings.

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Disaster Response and Research Reactivation

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Provides strategies and information pertinent to disaster response and research reactivation.

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Clery Act Training

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An in-depth review of the Clery Act and how higher education institutions can comply with applicable regulations.

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Clinical Trial Staff Diversity and Cultural Humility

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Discusses how clinical trial staff diversity and cultural humility can yield diverse subject recruitment and improved study outcomes.

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Title IX: 50 Years and Modern Challenges

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An in-depth review of the historical impact of Title IX and how to navigate modern challenges within higher education to ensure compliance.

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How to Conduct an Audit of a Ceded Study

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QA/QI professionals can learn to audit ceded studies for single IRB (sIRB) review.

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Drones in Academia

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Explores the use of drones in research and the regulations and requirements researchers and administrators need to know.

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Preparing for Success in Scholarly Publishing

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Foundational course that orients and prepares learners to engage with the scholarly publication process in an informed way.

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Understanding 483s and Surviving Them

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Discusses steps that investigators and clinical sites can take to understand and respond to an FDA Form 483.

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Managing Your Grants as Systems: A Guide for Grant Management Success

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Covers a systems approach to grant management and provides strategies for managing your team and your grant.

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Preparing to Publish in Traditional and Hybrid Journals

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Covers key concepts in scholarly publishing and provides an overview of the publication process for both traditional and hybrid...

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Data Management and Security for Student Researchers: An Overview

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Covers the best practices of data management and security for graduate student researchers.

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Protocol Development and Execution: Beyond a Concept

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An in-depth review of the development and execution of protocols.

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Race in Clinical Research: Ethics and IRB Decision Making

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Explores the concept of race in clinical research and important ethical and regulatory questions.

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Research Equity and the Part We Play

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Discusses ways to improve diversity and equity among clinical trial participants.

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U.S. DoD Regulations & Requirements for Human Subject Research

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Reviews DoD requirements and limitations for research.

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CRISPR Genome Editing: Rewriting DNA and the Future of Humanity

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Describes CRISPR genome editing, including its applications and ethical questions.

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Privacy and Ethics for Connected and Automated Vehicles

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An overview of connected and automated vehicles (CAVs) and the associated privacy and ethical challenges.

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Undue Foreign Influence: Risks and Mitigations

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Explore key ethical, export, security, intellectual property, and transparency requirements related to international engagement.

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Infection Prevention in Healthcare Settings

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Provides learners with a foundational understanding of infection prevention techniques.

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Laser Safety

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Meets the requirements of a general laser safety training program for research and medical institutions.

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General Laboratory Safety for Non-Laboratory Personnel

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Hazard awareness, communication, and safe practices for non-lab personnel working in and around laboratory facilities.

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FDA Inspections of GMP Facilities: How to Be Inspection Ready

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Discusses the FDA's approach to inspecting GMP facilities and the ways that facilities can prepare for inspections.

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ClinicalTrials.gov Enforcement: An Update

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Explores recent FDA enforcement of FDAAA 801 and noncompliance pitfalls to avoid.

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FCPA and University Research: What Faculty and Administrators Need to Know

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Reviews FCPA as it relates to university research.

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CRA Soft Skills, Time Management, and Effective Site Relationships

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Discusses the importance of CRA soft skills in building productive relationships with sites and sponsors.

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Improving the Clinical Trial Participant's Experience

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Discusses ways that sponsors, sites, and clinical research organizations can transform the clinical trial experience.

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Cost Allowability on Federally Sponsored Awards

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A review of allowability of expenditures on federally supported projects.

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IRB Review of Observational Research

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Explores different types of observational research and provides best practices for IRB review.

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Partnering with Technology Companies

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Provides an overall approach to and best practices for partnering with technology companies to design and conduct research.

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How to Effectively Manage a Research Administration Team

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Provides research administrators with strategies to build, improve, and retain employees.

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CTrials by BRANY

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CTrials helps grow sponsored research programs by taking on the many administrative challenges inherent in managing clinical trials.

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Protocol Builder

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Protocol Builder is an online protocol writing and collaboration platform that also speed up your pre-review turnaround times.

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Tech Software

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Tech Software a leading provider of SaaS compliance solutions for higher-education, academic medical centers, hospitals, government and biotech companies.

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The Network of Networks (N2)

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N2 is a not-for-profit alliance of Canadian research networks and organizations working to enhance national clinical research capability and capacity.

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BIC Study Foundation

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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.

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Browse Complete Catalog

Meet A Few Of Our Expert Authors and Presenters

Our courses are built by over 150 highly qualified experts and rigorously peer reviewed to incorporate various perspectives and ensure accuracy, completeness, and overall quality.

Content Contributor Wilbur Chen

Wilbur Chen, MD, MS, FACP, FIDSA

Center for Vaccine Development and Global Health, University of Maryland School of Medicine

Dr. Chen is an adult infectious disease physician-scientist with a specific interest in vaccines. He is Professor of Medicine at the University of Maryland School of Medicine and Director of the University of Maryland, Baltimore Travel Medicine Practice.

content contributor brandy nelson

Brandy Nelson is the University of Kentucky's Biosafety Officer. Brandy is a Certified Biosafety Professional, a Specialist in Microbiology, an Associate Safety Professional, and holds BA and MS degrees in Biology from Transylvania University and Eastern Kentucky University. Brandy has worked in biosafety for over 15 years.

content contributor jim gould

Jim Gould, PhD

Harvard Medical School

Dr. Jim Gould is Director of the Office for Postdoctoral Fellows and a Program Director of RCR Training at Harvard Medical School. He is a content expert on postdoctoral career and professional development, including career coaching, application material critique, job search advice, interview strategies, RCR, and navigating academia.

Content Contributor Roderick King

Roderick K. King, MD, MPH

University of Miami Miller School of Medicine

Roderick K. King, MD, MPH, is Senior Associate Dean for Diversity, Inclusion and Community Engagement and Director of the MD/MPH Program for the University of Miami Miller School of Medicine.

In Our Learners' Words

myrene m

Myrene M.

Associate Faculty

The course materials are brief and clear. Such brevity and clarity are perfect for those who are busy with other duties at work and provide for a more friendly and less overwhelming task. I love the quizzes because I can learn from my mistakes. After submitting the quiz, the correct and wrong answers are explained. This reinforces learning.

julie s

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.

folaasade a

Folasade A.

Student

I like the opportunity to be able to read/review CITI study notes at any time.

motunrayo o

Motunrayo O.

Professor

Very educative course. It was insightful and informative. I learned and relearned a lot.

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Courses Approved by a Top Academic CME Provider

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.

View CE Certified Courses

Recent News & Articles

New Webinar – How to Conduct an Audit of a Ceded Study

Content Update News

New Webinar – How to Conduct an Audit of a Ceded Study

The presenter will outline steps to set your QA/QI program up for success, including available resources and tools to support the auditing of ceded studies.

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What CITI Program is Reading – October 11th, 2022

Blog

What CITI Program is Reading – October 11th, 2022

"What CITI Program is Reading" is our weekly blog series which highlights news articles curated by our staff and relevant to research, higher education, healthcare,...

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Free Live Webinar – Successfully Navigating Subrecipient Monitoring

Upcoming Events

Free Live Webinar – Successfully Navigating Subrecipient Monitoring

Subrecipient monitoring is a federal requirement, but the regulations are often complex and confusing.

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Source: https://about.citiprogram.org/

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