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

Introduces a systematic method for analyzing safety statistics

An introductory video-based series to the DOE’s SBIR-STTR funding program and a discussion of key elements of the proposal elements.

This course explores explores technological advances and eConsults.

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

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

Provides learners with best practices for creating and maintaining study documents.

Covers how to identify red flags in your survey data, strategies to develop surveys to minimize fraud, and best practices for data management.

Understand CUI and the obligations it creates for universities and researchers.

Explores considerations for a human research protection program (HRPP) emergency preparedness plan.

Learn how to review nonexempt human subjects research protocols for regulatory compliance with the Common Rule.

Provides learners with key information on the management of controlled substances in clinical research settings.

This role-based course provides the practical know-how to monitor clinical research sites effectively.

This webinar reflects on the creation of a culture of compliance through the lens of how one university created an enterprise-wide compliance role.

Discusses what events must reported, to whom, and according to what timeline.

Learn about the FCPA and its impact to healthcare operations.

This webinar offers practical solutions for optimizing corporate board roles to foster a culture of ethics and compliance.

A role-based course that provides practical know-how to effectively lead or participate on data monitoring committees.

Overview of the European Union’s (EU) General Data Protection Regulation (GDPR).

Discusses the four pillars of a culture of care, the impact of compassion fatigue, and individual and institutional strategies to address compassion fatigue.

The webinar explores work-related musculoskeletal disorders among surgical teams.

An introduction to risk management and crisis response within study abroad programs.

An in-depth review of advanced topics important to research administrators.

Stress at research institutions is common, explore ways to navigate and mitigate the effects of stress in these settings.

This course focuses on promoting the success of international students on university campuses by offering strategies for academic support, cultural integration, and compliance with U.S. federal policies.

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.