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.
Provides pharmacists and pharmacy professionals with practical guidance on good pharmacy practices across retail, hospital, and clinical research settings.
Introduces the biological characteristics, animal care and health management practices, ethical considerations, and occupational safety practices relevant to working with cephalopods in research settings.
Examines practical strategies for recognizing and managing safety hazards in brewery operations.
Introduces action research as an ethical, iterative method for improving practice through planning, action, observation, reflection, and sharing findings in real-world settings.
This course provides researchers, institutional administrators, and IT professionals with the knowledge needed to safeguard CUI and meet federal compliance obligations.
Gain practical guidance on managing Dangerous Gain-of-Function Research (DGOF) and International Research of Concern (IROC) under the new U.S. Government Policy for High-Risk Life Sciences Research.
Explores the principles of research reproducibility and the intrinsic, environmental, and procedural factors that can influence the consistency and reliability of animal research.
Provides practical guidance for sharing biomedical research data ethically, responsibly, and in compliance with regulatory requirements.
This course provides a high-level overview of research misconduct definitions, procedures, and the roles and responsibilities of individuals who assist in the handling of an allegation.
Covers the ethical, regulatory, and practical considerations for using food‑producing animals in research, including veterinary oversight, biosecurity, regulated drug use, and food safety compliance.
This course covers expedited categories, helping IRB members and administrators identify minimal-risk studies, apply appropriate regulations, and make clear, consistent decisions.
Practical guidance for investigators on ClinicalTrials.gov registration, results reporting, review criteria, and ongoing compliance.
A comprehensive introduction to ethical principles, regulations, and responsible practices that guide software and technology professionals throughout the software development lifecycle.
Provides community research partners with disability-accessible education on ethical issues in social and behavioral research.
Prepares you to apply digital health ethics in healthcare and research.
This webinar examines responsible and ethical uses of artificial intelligence in research, including common misconceptions, governance frameworks, best practices, and key compliance considerations.
Learn practical strategies for effectively mentoring doctoral students through the dissertation process, from setting expectations to addressing common challenges and supporting successful completion.
Explains why bioethics departments are vital in HBCU medical schools and how confronting historical exclusion and health inequities can advance health justice through education, research, and community engagement.
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 introduces the essentials of healthcare compliance, including key fraud and abuse laws, Medicare billing, HIPAA, risk assessment, auditing, and the core elements of an effective compliance program.
Covers the ethical, regulatory, and practical considerations for using food‑producing animals in research, including veterinary oversight, biosecurity, regulated drug use, and food safety compliance.
Hands-on instruction on day-to-day practices of clinical research coordinators (CRCs).
Provides learners with the skills needed to create and manage controlled documents.
Explores practical strategies for preventing controlled substance diversion in vivarium settings, using real-world cases to help participants identify risk factors and implement effective prevention measures.
This course provides graduate students with practical guidance, strategies, and resources to confidently navigate each stage of the dissertation process from proposal to defense.
IP for Students and Postdocs introduces early-career researchers to intellectual property fundamentals, helping them identify, protect, and responsibly share innovations from academic and research settings.
Provides instructions for creating the structures, personnel, and funding for a clinical research program.
An introductory video-based series to the U.S. Department of War/U.S. Department of Defense SBIR-STTR funding program and a discussion of key elements of the proposal and proposal process.
Develop effective standard operating procedures for research administration with practical guidance on SOP writing, governance, version control, review, approval, and lifecycle management to improve consistency, usability, and process quality.
This webinar explores strategies for leading through rapid change in research administration and navigating evolving federal funding and policy landscapes.
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.
Amy Kenton has been a K-12 educator for over 30 years. She served in school and district leadership positions and taught graduate courses in educational leadership. Dr. Kenton serves on the Northwell Clinical Trials Participant Advisory Board and the Hofstra School of Education Advisory Board.
DVM from Kansas State University College of Veterinary Medicine. Completed a rotating internship and an MS in Analgesia and Anesthesia at Purdue University. Attending veterinarian at the Marine Biological Laboratory since 2017. Director of Marine Research Services since 2023.
Dr. Patrick Lester is a clinical professor in Laboratory Animal Medicine at the University of Michigan. Dr Lester is an experienced comparative medicine veterinarian and board-certified pharmacotherapy specialist pharmacist. Dr. Lester coordinates controlled substance activities for clinical veterinary services including use and management of automated dispensing cabinets.
Dr. Rachel Osborne, PharmD, is a clinical pharmacist with more than 20 years in the field of pharmacy. She has experience in community, hospital, and ambulatory care settings. Her background also includes working at a clinical research pharmacy and serving as a scientific member on an Institutional Review Board (IRB).
Pharmacy Student
The course provided detailed, relevant, real world examples of the historical influence on the regulations and previous failure to conduct ethical research.
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.
DSW Graduate Student
I enjoyed the comprehensive coverage of topics related to informed consent in the 21st century, including the use of technology in the consent process and federal guidance on multimedia tools and electronic consent forms.
College Research Professor
The course was clear and direct. It did not provide information that was unnecessary and confusing.
New Course – Good Pharmacy Practices
Provides pharmacy professionals with practical guidance for supporting patient safety, regulatory compliance, operational excellence, and clinical research across pharmacy settings.
Read the article
On Tech Ethics Podcast – Use of AI in Legal Discovery
Season 1 – Episode 50 – Use of AI in Legal Discovery Discusses the use of AI in the legal discovery process. Notes...
Read the article
Microbiology Devices Panel of the Medical Devices Advisory Committee Meetin...
The U.S. Food and Drug Administration (FDA) will host a hybrid meeting of the Microbiology Devices Panel of the Medical Devices Advisory Committee.
Read the article