Essential training covering preclinical to clinical research topics, including animal care and use, GCP, COI, human subject protections and IRB, and responsible conduct of research. Suitable for all types and sizes of organizations – from universities to academic medical centers to industry.
Provides core training in human subjects research and includes the historical development of human subject protections, ethical issues, and current regulatory and guidance information.
GCP consists of basic and refresher courses that provide essential good clinical practice training for research teams involved in clinical trials.
RCR covers core norms, principles, regulations, and rules governing the practice of research.
These courses cover the general principles of the ethical care and use of animals in research, training, and testing.
The Conflicts of Interest and Commitment series contains a number of COI courses of interest to organizations.
IPS covers data protection principles, focusing on basic information security requirements and the educational records and data-related requirements of FERPA.
*A “site” is a facility owned and/or operated by or actively affiliated with a subscribing organization where 30 or more employees, agents, or students of the organization will complete CITI Program courses in a given year. Large organizations with a high learner volume, virtual learner groups, healthcare systems, science fair organizations, and other complex organizations may be considered equivalent to multiple sites. Each site shall be required to pay a CITI Program base subscription fee. Due to the increasing trend in organizational and site mergers, we want to remind our institutions that a merger does not result in two base subscriptions becoming one, since our costs of supporting these current and future learners typically do not change. Please contact us to discuss your organizational subscription needs.
Individuals who are not affiliated with a subscribing organization can purchase courses online (learn more).