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

This course provides a practical introduction to U.S. export control requirements.

This course provides a high-level overview of research misconduct definitions, procedures, and the roles and responsibilities of individuals who assist in the handling of an allegation.

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.

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

This webinar explores cybersecurity risks in faculty–student collaborative research, with a focus on protecting sensitive research data, meeting sponsor cybersecurity requirements, and applying institutional security controls and best practices.

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

This webinar helps trainees and early‑career investigators understand grant application review processes, scoring criteria, and common reasons proposals are not funded.

This webinar explores work-life balance challenges in research administration and presents strategies to reduce burnout, improve efficiency, and support compliant research operations.

This webinar explores replication’s role in scientific progress and public trust, covering the replication crisis, how replications are evaluated, and barriers to making them routine.

Provides an overview of research security requirements and researcher responsibilities and best practices.

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

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

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

This course provides information on IATA and DOT packaging/shipping requirements.

The Conflicts of Interest and Commitment series contains a number of COI courses of interest to organizations.

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

This course offers training on post-approval monitoring.

This course provides training on good laboratory practice for non-clinical laboratory studies that reflects regulations and best practices established by key regulatory agencies and guidelines.

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

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

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

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.

Provides an overview of successful remote monitoring across clinical research, clinical care, and public health.

CRC courses focus on key topics essential to the conduct of clinical research. They are specifically tailored to the needs of clinical research coordinators.

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.