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

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

IP for Students and Postdocs introduces early-career researchers to intellectual property fundamentals, helping them identify, protect, and responsibly share innovations from academic and research settings.

Introduces document control principles, Good Documentation Practices, and responsibilities of lead document controllers.

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

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

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

This course offers practical training on ICD-10-CM structure, coding conventions, and official guidelines to support accurate diagnosis coding, proper billing, and audit readiness across leadership roles.

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

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

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

Describes the regulatory framework and quality programs for HCT/Ps

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

Explores how generative AI (GenAI) can support science communication.

Describes how to calculate the appropriate sample size for different study designs and outcomes.

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.

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

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.

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

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.