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

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

This webinar gives residents, fellows, and faculty an overview of common clinical research funding paths and practical tips for crafting strong, fundable proposals.

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.

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

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.

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.

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.

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.

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.

Explains why and how IRBs must assess quantitative research design as an ethical issue, including risks like poor methodology, participant burden, data privacy, and AI-generated data contamination.

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.