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GCP for Clinical Investigations of Drugs and Devices (FDA)
Ideal for individuals proposing to conduct clinical trials of drugs, biologics, and devices primarily in the U.S.
Revised Common Rule: Overview of Revisions
It has been more than six months since the revised Common Rule’s implementation date, revisit the revisions it made using thi...
Revised Common Rule: Revisions to Definitions
In-depth review of revisions to the definitions section of the Common Rule. Covers new terms added, updates to existing definit...
Revised Common Rule: Revisions to Informed Consent
Explores the revised Common Rule’s updates to informed consent. Focuses on key changes, new elements, and updates to existing...
Participating in Vaccine Research (Free Webinar)
Learn about what to expect when participating in vaccine research.
IRB Member – Biomedical Focus
Provides foundational training for IRB members involved in the review of biomedical human subjects research.
IRB Member – Biomedical and Social-Behavioral-Educational Combined
Provides foundational training for IRB members involved in the review of both biomedical and social-behavioral-educational huma...
IRB Administrator Professional Development and Self-Advocacy
Learn how to grow and develop yourself as an IRB administrator.
On Research Podcast - PRIM&R 2023: Insights and Takeaways
Season 1 - Episode 13
This is a special edition of On Research with CITI Program. Guest hosted by Margaret Rankovic, Director of Content and Education at CITI Program, this podcast provides a recap, insights, and key takeaways from the recently concluded PRIM&R 2023 conference.
