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

This course introduces the essentials of healthcare compliance, including key fraud and abuse laws, Medicare billing, HIPAA, risk assessment, auditing, and the core elements of an effective compliance program.

Practical guidance for investigators on ClinicalTrials.gov registration, results reporting, review criteria, and ongoing compliance.

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.

This course covers expedited categories, helping IRB members and administrators identify minimal-risk studies, apply appropriate regulations, and make clear, consistent decisions.

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

Provides essential training on why privacy awareness and compliance matter.

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

Covers the NIH SBIR-STTR proposal process, from program eligibility and proposal development to submission, award implementation, and business-university partnerships.

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

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

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

Covers the ethical, regulatory, and practical considerations for using food‑producing animals in research, including veterinary oversight, biosecurity, regulated drug use, and food safety compliance.

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.

This webinar outlines key requirements, exceptions, and compliance steps under the NIH Policy on Enhancing Security Measures for Human Biospecimens.

This webinar outlines key requirements, exceptions, and compliance steps under the NIH Policy on Enhancing Security Measures for Human Biospecimens.

Explains how AI can be responsibly integrated into GMP auditing to enhance audit execution, data integrity, and compliance while anticipating emerging regulatory and risk considerations.

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.

A detailed review of radiation safety for research and medical institutions.

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.