Research Ethics and Compliance Training
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Biomedical PI
Review the important role of the biomedical investigator in a clinical investigation that complies with federal regulations and GCP standards.
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Protocol Registration and Results Summary Disclosure in ClinicalTrials.gov
A video-enhanced practical guide to compliance with protocol registration and summary results reporting.
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Transitioning Research to the Revised Common Rule: The What, How, and Why
Learn about transitioning pre-existing research to the revised Common Rule, required documentation, and tips
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for IRB review. -
Semiannual Evaluations In Depth
Maintain a high-quality animal care and use program at your organization.
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If you are not affiliated with a subscribing organization, you can register as an independent learner.
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A base subscription includes all core subjects and an unlimited number of users at your primary facility or campus. Ask about special pricing for additional facilities.
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Protocol Builder makes the protocol-writing process more efficient
Join a live webinar to learn about the latest platform enhancements:
- Revised Common Rule guidance updates - for biomedical and social behavioral protocol templates
- Protocol template customization
- IRB submission tracking
Next webinar on Thursday 4/18 at 3:30pm EST.
New Course Available: Biomedical PI
Learn about key topics essential to the biomedical investigator’s role and responsibilities in conducting a clinical investigation of a product regulated by the FDA.
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February 2019 Newsletter
We invite you to review our February 2019 newsletter which discusses bioethics, new and updated content, GDPR violations, study design and reproducibility, current administrator support topics, and resources from our partners.
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21-23 May 2019 - AAHRPP Annual Conference
AAHRPP's annual conference brings together research professionals and organizations dedicated to quality research, to discuss topics in human research protection.
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