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Content suggestions provide CITI Program with a way to stay in tune with the emerging issues and concerns important to the research, ethics, and compliance communities. We value your opinions and invite you to submit your content ideas below. All suggestions will be explored and considered by our content team and will remain anonymous.

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Our courses are developed by experts and are rigorously peer reviewed to incorporate various perspectives and to ensure accuracy, completeness, and overall quality. We welcome nominations for subject matter experts to join our author and peer reviewer groups. Please complete the form below to submit your nomination.

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Subscribe or resubscribe to our CITI Program account administrator email list and receive weekly updates including new content releases, live webinar registrations, other important account notifications, and more.

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Learning

Are You Thinking About Being in a Research Study?

Before deciding to participate in a research study or clinical trial, you should learn about what to expect and where to find more information. This resource covers subject’s rights, questions that should be asked about the study, informed consent, and definitions of commonly used terms.

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Coronavirus (COVID-19) Resources

CITI Program has compiled these resources to help the research community prepare for and manage the challenges presented by outbreak of COVID-19. We will update this list with important news including arising issues and regulatory updates.

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Revised Common Rule Updates to Informed Consent

Download this review of the basic and additional elements of informed consent per 46.116(b) and 46.116(c) in the Revised Rule.

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Organizations

BRANY (Biomedical Research Alliance of New York)

BRANY is the leading provider of research support services to hospitals, academic medical centers, and investigators. Staffed by multi-disciplinary experts, BRANY is an expedited “end-to-end solution” for clinical trials. Offerings include single IRB (sIRB), Social Behavioral IRB (SBER IRB) and Medicare Coverage Analysis.

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HRP Consulting Group (HRP): Research and Ethics Consulting

With over 150 years of combined experience in human research protections, HRP provides services including the development of human research protections programs, training and education, assistance with accreditation, IRB administration and auditing.

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Tools

Protocol Writing Technology

Protocol Builder® reinforces best practices for developing clinical research protocols taught by CITI Program. This secure cloud-based technology helps ensure quality and consistency so protocols can move through internal and IRB review processes more efficiently. Special pricing is available to CITI Program organizational subscribers.

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Regulatory Binder Tabs

This set of regulatory binder tabs is intended to help principal investigators (PIs) and research teams organize the information that is required to be retained in the course of their clinical research study. While you may use electronic systems or a mix of paper and electronic systems, it is very beneficial to have a central “repository” that details where and how everything can be found.

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