The Trusted Standard in Research, Ethics, Compliance, and Safety Training

These courses explore key topics related to research security and international engagement.

A foundational course that teaches researchers to fully integrate qualitative and quantitative approaches for rigorous, ethical, high-quality mixed methods research.

Equips research personnel with the skills and insights necessary for effective mentorship.

This course offers advanced training for experienced researchers and leaders in responsible research conduct, emphasizing integrity, ethical leadership, and fostering healthy research environments.

This course prepares researchers and educational technology developers to navigate COPPA’s legal requirements, conduct compliant research, and engage with digital environments used by children under 13.

This course equips community partners with the knowledge and skills to ethically and effectively engage in research.

The IRB Review of Exempt Research course provides an overview of the exempt categories of research per 45 CFR 46.104 and discusses considerations for making an exempt determination per regulatory criteria.

An introductory video-based series to the NSF’s SBIR-STTR funding program and a discussion of key elements of the proposal and proposal process.

This course provides training on working with insects in research settings.

Covers various considerations for reviewing human subjects research, including subject selection, risk minimization, balancing risks and benefits, and privacy and confidentiality.

Provides hands-on knowledge of research accounting principles and practices.

Introduces you to key information about, and tools to use, the 3Rs of animal research.

Prepares you to apply digital health ethics in healthcare and research.

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

Explores how behavioral science can enhance compliance programs.

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

This course provides learners with a review of contemporary bioethics issues.

Provides learners with an understanding of environmental regulations affecting the biotech industry.

Provides learners with best practices for maintaining document control in a research setting.

Explores underutilized IRB exemptions and highlights flexible approaches, especially in categories 4 through 8, through discussion and real-world examples.

This webinar for IRB, IACUC, and sponsored program administrators covers seven key compliance elements with strategies and case studies to strengthen research, reduce risk, and promote integrity.

Explores how researchers and IRB reviewers can collaborate to navigate the complexities of research involving youth.

An in depth look at the federal Title IX law and required compliance of faculty, staff, and administrators.

This course equips faculty, staff, and administrators with the fundamentals and tools to measure outcomes, improve learning, and effectiveness.

Provide your organization's learners with access to currently available and future webinar recordings.

Provides a foundational overview of quantitative methods, equipping learners with the essential tools to analyze and interpret numerical data for research and decision-making.

An overview of PCTs, their ethical complexities, best practices, and institutional considerations.

Provides instruction on how to improve your teaching and training skills in a variety of settings.

Provides an overview of conflict, types of conflict, conflict styles, communication styles, and intervention strategies.

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.

A complete research compliance suite that supports IRB, IACUC Conflict of interest, Bio Safety Export Control, and more.

HRP Consulting provides customized services for your research program, including temporary staffing, IRB/IACUC assistance, accreditation support, program evaluations, training/education and more.

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.