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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IACUC Administration
A concise review of IACUC administration, perfect for both new and experienced IACUC administrators.
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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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Building a ClinicalTrials.gov Compliance Program – Tips for Investigators and Institutions
Learn about the regulations, important timelines, agency-specific variances, and a range of compliance mechanisms.
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Laboratory Chemical Safety
Learn the fundamental safety practices for working with hazardous chemicals in the laboratory.
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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 Course Available: Compensation Reporting
Add our newest course on compensation reporting requirements and best practices. It is ideal for individuals who work with federally sponsored awards, principal investigators, and other members of the research team.
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Improving Drugs Through Patient-Centric Design for Clinical Trials
Read about the approach to drug development that includes tolerability, ease of use, compliance with therapy, and quality of life as topics addressed along with traditional quantitative risk-benefit analysis. The author speaks to the need for new and creative solutions that address the broader needs of patients as individuals. Improving the next generation of drugs […]
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9-12 February 2020 - 14th Clinical Trial Billing & Research Compliance Conference
Interact with Research Billing Compliance experts to develop strategic partnerships by finding the balance between coverage analysis, adequate budgets, and revenue integrity.
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