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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Utilized by the Top-25 Best National Universities*
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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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Over 10 Million Learners with 19+ Million Course Completions
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95% of Carnegie R1 Research Universities are 10+ year subscribers

Explore Our Course Catalog

Biotility: Good Documentation Practices (GDP)
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Strategies for implementing compliance with GDP, as well as standards and procedures for accurately completing Records required for current cGMP.

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Biotility: Corrective Action Preventive Action (CAPA)
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Describes regulatory requirements for a CAPA system in the biotech industry.

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Biotility: Regulatory Approval for Medical Devices (United States)
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Describes FDA’s regulatory controls for common marketing approval pathways for the classes of medical devices, and explains the Code of Federal Regulations that pertain to medical device approval in the U.S.

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Biotility: cGMP for Dietary Supplements
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Explains requirements to establish and maintain regulatory compliance with 21 CFR Part 111 cGMP in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements.

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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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Best Practices for Global Research Partnerships: Benefits and Challenges
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Reviews best practices and challenges for navigating collaborative research partnerships in a global environment.

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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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Bring Your Own Device (BYOD) Studies
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Discusses BYOD study best practices, implementation, and Institutional Review Board (IRB) review.

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Good Manufacturing Practices (GMP)
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An in-depth introduction to GMP for pharmaceuticals.

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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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Technology Transfer
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An introduction for researchers on university technology transfer and commercialization processes.

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FDA Inspections: From Site Preparation to Response
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Covers regulatory inspections of clinical investigators and sites, including mock inspections, 482s, 483s, warning letters, communication, and CAPA plans.

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Working with Your IRB
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Strategies to work with your reviewing IRB.

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Facial Recognition Considerations for Researchers
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Covers the use of facial recognition systems in research and healthcare.

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Communicating Research Findings
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This course focuses on effective practices, guidelines, and strategies for communicating and presenting research findings.

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Family Educational Rights and Privacy Act (FERPA)
CME/CEUFeatured

This course covers the core requirements of the federal Family Educational Rights and Privacy Act (FERPA).

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Healthcare Ethics Committee (HEC)
CME/CEUFeatured

This course focuses on developing the knowledge and skill base necessary for being a successful healthcare ethics committee member.

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Responsible Conduct of Research (RCR) Basic
CME/CEUFeatured

This course covers the core norms, principles, regulations, and rules governing the practice of research.

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Title IX and the New Regulations
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Discusses key elements of the new 2020 regulations, how they affect the institutional community, and what you should know to implement best practices into revised Title IX procedures and policies.

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IRB Protocol Noncompliance: When Research Goes Rogue, What Next?
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Discusses strategies to address researcher noncompliance with IRB-approved protocols.

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Radiation Safety
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A detailed review of radiation safety for research and medical institutions.

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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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False Claims Act: A Primer and Guide for Research Organizations
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This course provides an introduction to the False Claims Act ideally suited for faculty, researchers, and staff at research organizations.

False Claims Act: A Primer and Guide for Research Organizations
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Compensation Reporting (Effort Reporting)
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A focused discussion for individuals who work with federally sponsored awards, PIs, and other members of the research team.

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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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A Beginner’s Guide to Being a Sponsor-Investigator
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A primer for understanding the sponsor-investigator role and responsibilities in clinical research.

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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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Teaching and Training for Professionals
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Provides instruction on how to improve your teaching and training skills in a variety of settings.

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Disaster Planning for the Research Enterprise
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This course offers information about disaster planning and business continuity to those responsible for research oversight.

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Essentials of Research Administration
CME/CEUFeaturedUpdated

This course provides an overview of research administration.

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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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see offering
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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see offering
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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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 150 highly qualified experts and rigorously peer reviewed to incorporate various perspectives and ensure accuracy, completeness, and overall quality.

EAB member Ada Sue Selwitz

Ada Sue Selwitz, MA

University of Kentucky

Ada Sue Selwitz MA assists the University of Kentucky in developing policies and educational programs pertaining to research compliance, advises on regulations and research ethics, and serves on NIH funded grants. She is Associate Director of Regulatory Support for the Center for Clinical and Translational Sciences and a SmartIRB Ambassador.

Content contributor alisha oropallo

Alisha Oropallo, MD, FACS, FSVS, FAPWCA

Northwell Health

Alisha Oropallo, MD FACS, Director of the Comprehensive Wound Healing Center. She is an Associate Professor at Zucker Hofstra School of Medicine and Feinstein Institutes of Medical Research. She has been the lead investigator on clinical trials, published papers, and has been invited to lecture in wound healing globally.

Content Contributor Tim Bacon

Tim Bacon, BA

Medicine in Practice Inc.

Tim Bacon is CEO of Medicine in Practice, an organization dedicated to providing training for clinical research teams. Tim is a Founding Member of the International Society for Medical Publication Professionals (ISMPP), served as its inaugural Chair, and subsequently led the credentialing committee.

Content Contributor Mitchell Parrish

Mitchell Parrish, JD, RAC, CIP

H Clinical

Mitchell is the President of H Clinical. With a 15-year passion for enabling clinical research, supporting life sciences, and transforming organizations, Mitchell is responsible for H Clinical’s strategy, business activities, and operations. Prior to H Clinical, Mitchell served as Managing Director, Everglade Rx, Executive VP & General Counsel, Advarra, and Associate Attorney, K&L Gates.

In Our Learners' Words

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.

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.

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

CITI Program and Biotility at University of Florida Announce Partnership
Content Update News

CITI Program and Biotility at University of Florida Announce Partnership

Agreement will leverage complementary expertise in the biotech industry and higher ed online learning

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What CITI Program is Reading – May 17, 2022
Blog

What CITI Program is Reading – May 17, 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 – A 21st Century Approach to ADA Compliance: Equity and Access
Upcoming Events

Free Live Webinar – A 21st Century Approach to ADA Compliance: Equity and Access

In this webinar, we will explore strategies to address the inequities that exist within research practices to ensure the ethical inclusion of subjects in clinical trials.

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