The synergistic relationship between best practices, regulations, and professional experience forms the foundation for working in a BSL-3 facility.

Learn how to review nonexempt human subjects research protocols for regulatory compliance with the Common Rule.

This course covers controlled substance use in analytical and animal research, offering an overview of relevant federal regulations for research personnel.

Describes ways to overcome difficulties in study start-ups.

After the rigor of completing funding applications, this webinar discusses various tactics for success post-award.

Explores ethical and regulatory considerations for human subjects research in outer space.

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Learn about the FCPA and its impact to healthcare operations.

Covers the principles, governance approaches, practices, and tools for responsible artificial intelligence (AI) development and use.

AI is always evolving and this webinar will go over the (current) basics of artificial intelligence in relation to academic and research integrity.

Explores the importance of ethics for AI companies and its impact on public trust and profitability.

This course focuses on developing the knowledge and skill base necessary for being a successful healthcare ethics committee member.

This course covers the core norms, principles, regulations, and rules governing the practice of research.

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Foundational course covering the core components of pharmacovigilance and materiovigilance.

This course teaches a systematic approach to investigating quality issues, creating effective corrective action plans rooted in...

This advanced, role-based course provides second-level training tackling topics of importance for experienced IRB administrators and HRPP directors.

This course provides foundational training on conflicts of interest for healthcare professionals.

This course provides necessary insight to understand, distinguish, and perform the spirit of the law as described in ADA of 1990 and 2003 and other relevant laws for compliance purposes.

Discusses the process and content of a CRA’s interim monitoring visit.

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This course covers lean manufacturing as a production process based on an ideology of maximizing productivity while simultaneously minimizing waste within a manufacturing operation.

Learn strategies for promoting equity, diversity, and inclusivity in clinical research participation.

Details ways to produce productive partnerships between clinical research associates and clinical research coordinators.

This webinar looks at sources of burnout in higher education, national datasets, and recommendations for increasing employee wellbeing.

Describes how to apply the Lean Six Sigma principles to research administration process improvements.

Explains how to facilitate an open discussion on research integrity using the Dilemma Game App.

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CTrials helps grow sponsored research programs by taking on the many administrative challenges inherent in managing clinical trials.

Informed Consent Builder is a cloud-based platform that streamlines the process of managing and generating informed consent forms.

Protocol Builder is an online protocol writing and collaboration platform that also speed up your pre-review turnaround times.

N2 is a not-for-profit alliance of Canadian research networks and organizations working to enhance national clinical research capability and capacity.

BIC Study Foundation is a resource for those who want to take CITI Program courses in Korean. They are a certified training provider by the Korean FDA/MAFRA for HRPP and ACU Programs.