Research Ethics and Compliance Training
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Compensation Reporting
Explore the requirements of and compliance with compensation reporting on federal awards.
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Running a Virtual IRB Meeting
Identify strategies for running an IRB meeting in a virtual environment, addressing key areas for IRB chairs, members, and staff.
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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.
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Laboratory Chemical Safety
Learn the fundamental safety practices for working with hazardous chemicals in the laboratory.
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Understanding Consent Requirements and “Key Information” Under the Revised Rule
Explore the informed consent requirements related to increasing understandability and
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“Key Information." -
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.
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All Access Webinar Package
Access all of CITI Program’s currently available webinar recordings as well as future recordings released during your subscription period.
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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 NOWSubscribe 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.
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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.
New Webinar: Understanding Consent Requirements and “Key Information” Under the Revised Rule
Review new regulatory requirements, learn to develop effective consent materials, and explore "key information" for different types of research.
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U.S. Federal Regulatory Agencies Provide Guidance for Clinical Trials in Response to COVID-19
As COVID-19 continues to impact research organizations and clinical sites, federal agencies are issuing guidance for clinical trials. Organizations are closing or dramatically reducing operations and on-site staff; supply chains are disrupted; and travel restrictions have left investigators, organizations, and sponsors scrambling to respond. In response, the FDA is providing guidance for those impacted. The […]
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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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