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.
Foundational course covering the core components of the clinical research enterprise.
An in-depth course to train IACUC members on conducting protocol reviews.
Covers a systems approach to grant management and provides strategies for managing your team and your grant.
Describes CRISPR genome editing, including its applications and ethical questions.
Provides a review of GSM communities and important considerations when members participate in research.
Covers the best practices of data management and security for graduate student researchers.
Discusses BYOD study best practices, implementation, and Institutional Review Board (IRB) review.
An in-depth introduction to GMP for pharmaceuticals.
An in-depth review of the development and execution of protocols.
An introduction for researchers on university technology transfer and commercialization processes.
Covers regulatory inspections of clinical investigators and sites, including mock inspections, 482s, 483s, warning letters, communication, and CAPA plans.
Covers the use of facial recognition systems in research and healthcare.
This course focuses on effective practices, guidelines, and strategies for communicating and presenting research findings.
This course covers the core requirements of the federal Family Educational Rights and Privacy Act (FERPA).
This course focuses on developing the knowledge and skill base necessary for being a successful healthcare ethics committee member.
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.
Discusses strategies to address researcher noncompliance with IRB-approved protocols.
A detailed review of radiation safety for research and medical institutions.
Explore key ethical, export, security, intellectual property, and transparency requirements related to international engagement.
This course provides an introduction to the False Claims Act ideally suited for faculty, researchers, and staff at research organizations.
A focused discussion for individuals who work with federally sponsored awards, PIs, and other members of the research team.
Foundational course that orients and prepares learners to engage with the scholarly publication process in an informed way.
A primer for understanding the sponsor-investigator role and responsibilities in clinical research.
Provides an overall approach to and best practices for partnering with technology companies to design and conduct research.
Provides instruction on how to improve your teaching and training skills in a variety of settings.
This course offers information about disaster planning and business continuity to those responsible for research oversight.
This course provides an overview of research administration.
CTrials helps grow sponsored research programs by taking on the many administrative challenges inherent in managing clinical trials.
Protocol Builder is an online protocol writing and collaboration platform that also speed up your pre-review turnaround times.
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.
Highlighted below are just a few select subscribers & collaborators.
New Webinar – Managing Your Grants as Systems: A Guide for Grant Management Success
This webinar takes a systems approach to grant management. It outlines a process to identify components of your particular systems approach.Read the article
Recap of New OLAW Guidance and USDA Regulatory Updates
The Public Health Service (PHS), Office of Laboratory Animal Welfare (OLAW) recently published guidance on flexibilities for the conduct of semiannual animal facility inspections as...Read the article
Join the NIH and OHRP for a Conversation About Single IRB
Join the National Institutes of Health (NIH) and the Office for Human Research Protections (OHRP) for their January 2022 SMART Talk: A Conversation with NIH...Read the article