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Skip Navigation +1 888.529.5929 English Español 한국어 Português 中文 Русский 日本語 français tiếng Việt Register Log In -- Español 한국어 Português 中文 Русский 日本語 français tiếng Việt -- +1 888.529.5929 Register Log In MENU MENU Subscriptions Organizational Subscriptions Setting Up CITI Program Learners: How to Take Courses CITI Program Advantages Courses View All CE Certified Courses Animal Care and Use (ACU) Bioethics Biomedical PI Biosafety and Biosecurity (BSS) Clinical Research Coordinator (CRC) Clinical Trial Billing Compliance (CTBC) Compensation Reporting Conflicts of Interest (COI) Disaster Planning for the Research Enterprise (DPRE) Essentials of Grant Proposal Development Essentials of Research Administration Essentials of Statistical Analysis (EOSA) Export Compliance (EC) False Claims Act: A Primer and Guide for Research Organizations Good Clinical Practice (GCP) Good Laboratory Practice (GLP) Healthcare Ethics Committee (HEC) Human Subjects Research (HSR) IACUC Administration Information Privacy & Security (IPS) IRB Administration Laboratory Chemical Safety Protocol Registration and Results Summary Disclosure in ClinicalTrials.gov Research Study Design Responsible Conduct of Research (RCR) Semiannual Evaluations In Depth Webinars View All Courses Tools Support Support Center FAQ Sales Center CE/CMEs Research Ethics and Compliance Training False Claims Act: A Primer and Guide for Research Organizations Explore the False Claims Act and Civil Monetary Penalties Law. View Course Understanding Consent Requirements and “Key Information” Under the Revised Rule Examine the informed consent requirements related to increasing understandability and “Key Information." View Webinar BRANY SBER IRB Services Social, behavioral, and educational research has its own set of unique needs, and we understand them. Find out more about the SBER expertise, experience, and unique connected model of our accredited IRB. Learn More Compensation Reporting Explore the requirements of and compliance with compensation reporting on federal awards. View Course Medical Marijuana: A Budding Field of Research Discuss unique challenges and issues as well as considerations for IRB review and steps for getting started in medical marijuana research. View Webinar Laboratory Chemical Safety Learn the fundamental safety practices for working with hazardous chemicals in the laboratory. View Course Essentials of Grant Proposal Development Take the mystery out of grant writing with in-depth instruction that includes videos, exercises, resources, and examples. View Course Bioethics Gain a contemporary understanding about major bioethics concepts, principles, and issues. View Course All Access Webinar Package Access all of CITI Program’s currently available webinar recordings as well as future recordings released during your subscription period. View Package Essentials of Public Health Research Learn about the structure and function of public health systems, differentiate research and practice, and review consent and ethical issues. View Course Clinical Research Coordinator Engage in foundational and advanced role-based training for clinical research professionals. View Courses Communicating Research Findings Focuses on effective practices, guidelines, and strategies for communicating and presenting research findings. View Course Register to take courses developed by experts If you are not affiliated with a subscribing organization, you can register as an independent learner. GET STARTED NOW Subscribe your organization to CITI Program training A base subscription fee includes unlimited access to all core subjects for learners at each of your organization’s sites. Inquire about pricing for additional facilities and large institutions. LEARN MORE CITI Program Subscribers: Protocol Builder Special Offer Sign up for an informational webinar to learn more about Protocol Builder. The online protocol-writing application helps investigators write better quality SBER and NIH protocols and includes training resources for new investigators and residents. Our Special Offer for CITI Program Subscribers: Research Study Design course included with 3-year Protocol Builder subscription. Request A Webinar Content Update News New Course - False Claims Act: A Primer and Guide for Research Organizations This course provides an introduction to the False Claims Act that is ideally suited for faculty, researchers, and staff at research organizations. Learn More Blog Webinar - COVID-19 and Human Research Protection Programs Presented by Brenda L. Ruotolo, BA – Columbia University; Challace D. Pahlevan-Ibrekic, MS – Columbia University. An in-depth discussion on how one institution and its HRPP responded to the COVID-19 pandemic that may help guide other organizations. Webinar Highlights Provides a detailed exploration of how a human research protection program (HRPP) responded to and has […] Learn More Upcoming Events 5-7 April 2020 - PRIM&R IACUC Conference Attendees will learn about ethical issues and the federal regulations governing animal care and use, best practices for the review and monitoring of research that includes animals, and other timely and late-breaking topics. 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