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

This course provides graduate students with practical guidance, strategies, and resources to confidently navigate each stage of the dissertation process from proposal to defense.

Provides learners with an examination of developments in ICH Good Clinical Practice.

Describes how to build a fit-for-purpose regulatory strategy that strengthens your business strategy and differentiates your product in today’s digital health market.

The course provides fundamental knowledge of the principles and practices of clinical research.

Covers various considerations for reviewing human subjects research, including subject selection, risk minimization, balancing risks and benefits, and privacy and confidentiality.

Provides a foundational overview of quantitative methods, equipping learners with the essential tools to analyze and interpret numerical data for research and decision-making.

Explains how the Common Rule applies to secondary research with data and biospecimens.

Teaches you how to develop, evaluate, and deploy a digital measurement product that meets the requirements of regulators and payers, as well as your buyers and adopters.

An introduction for medical students of the essential considerations in planning and conducting research.

Foundational overview of clinical research meant to prepare medical residents and fellows to conduct their own research and work on research teams.

Discusses regulations and emergency response considerations for colleges and universities with research reactors, nuclear chemistry programs, and linear accelerators.

A video-enhanced guide to compliance with the FDAAA Final Rule and NIH Policy on clinical trial disclosure.

A thorough review of the Belmont Report’s principles, their evolution, and their application to research with humans.

Prepares you to apply digital health ethics in healthcare and research.

Provides an introduction to open science principles and practices.

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

Introduces the basics of planning for, managing, sharing, and archiving data generated through biomedical research involving human participants.

Provides an introduction to the EU AI Act, including risk-based approaches, compliance obligations, enforcement, interplays with other European digital policy, and perspectives

Provides learners with best practices for maintaining document control in a research setting.

Reviews the elements of the Common Rule’s exemption categories.

A detailed review of the IRB meeting and membership requirements.

This course offers a foundational overview of the critical areas associated with IRB and IRB office operations.

Identifies the key elements of the ORI Final Rule on Research Misconduct and explores how to implement these changes in institutional policies.

Provides hands-on knowledge of research accounting principles and practices.

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.

This course introduces school-based telehealth and explores ways to implement and evaluate these programs.

This course provides an in-depth overview of best practices and strategies for successfully enrolling international students, while focusing on federal policies.

Covers the essentials of statistical analysis to help learners gain greater statistical literacy.

This course covers lean manufacturing as a production process based on an ideology of maximizing productivity while simultaneously minimizing waste within a manufacturing operation.

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.