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

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

Provides community research partners with disability-accessible education on ethical issues in social and behavioral research.

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

Provides learners with an understanding of the principles of inventory management.

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.

An introductory video-based series to the U.S. Department of War/U.S. Department of Defense SBIR-STTR funding program and a discussion of key elements of the proposal and proposal process.

Serves as research security training designed to augment RECR/RCR training.

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

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

Provides essential training on why privacy awareness and compliance matter.

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.

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.

Practical information on the fundamentals of being a Principal Investigator (PI).

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

This webinar explains the DOJ Bulk Data Transfer Rule, its key requirements, and how data mapping supports compliance with NIH biospecimen security expectations.

This series provides a comprehensive overview of cybersecurity in healthcare, exploring organizational strategies, technical defenses, and risk management practices to safeguard data, operations, and trust.

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.

Describes the regulatory framework and quality programs for HCT/Ps

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

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

Helps clinical and operations leaders move from AI exploration to confident, ethical, and effective implementation.

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

Explores practical, ethical, and regulatory strategies for designing and reviewing research involving younger populations, emphasizing risk mitigation, regulatory flexibility, and effective collaboration between researchers and IRBs.

Presents a scalable model for creating a research coordinator float pool to provide flexible staffing, structured training, and broad support for clinical research across institutions.

Explores the benefits and the considerations of working with consultants on research misconduct investigations.

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.