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

Provides instructions for creating the structures, personnel, and funding for a clinical research program.

Provides essential training on why privacy awareness and compliance matter.

A comprehensive introduction to ethical principles, regulations, and responsible practices that guide software and technology professionals throughout the software development lifecycle.

The course explores OPSEC in academia, training faculty, staff, and students to identify and mitigate risks to sensitive research data while upholding open science principles.

Equips university faculty, staff, administrators, and students with essential knowledge on Title IX compliance and program assessment to foster safer, more effective, and student-centered campus environments.

Helps clinical and operations leaders in safety-net and low-resource healthcare settings develop literacy and confidence in AI.

Provides a review of what COI committee members need to know.

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

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

The RCR Casebook course is a collection of real-world ethical dilemmas designed to promote discussion, critical thinking, and skill-building in RCR.

Explore the impact of academic integrity from the perspective of both students and faculty/staff.

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

Explores issues that lead to research misconduct and ways to develop trust with faculty and leadership.

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.

Foundational and advanced courses provide critical information and best practices for IRB administration.

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.

Describes the regulatory framework and quality programs for HCT/Ps

This course provides essential practices for those working with high-risk biological materials, clarifying biosafety vs. biosecurity and enabling practical biosecurity planning to prevent theft, misuse, or intentional release.

The webinar explores effective collaboration between IACUC and IBC, detailing their roles, regulatory responsibilities, and best practices to ensure safe and ethical life sciences research while enhancing oversight and protecting workers and animals.

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

Provides the fundamentals of ergonomics across different settings.

Helps develop leadership skills to meet today’s changing, diverse, and dynamic environments.

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

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.