Foundational course covering the essential components of medical monitoring.

Strategies for implementing compliance with GDP, as well as standards and procedures for accurately completing Records required for current cGMP.

Describes FDA’s regulatory controls for common marketing approval pathways for the classes of medical devices, and explains the Code of Federal Regulations that pertain to medical device approval in the U.S.

Covers key concepts in scholarly publishing and provides an overview of the publication process for both traditional and hybrid...

Learn about the NIH Data Management and Sharing Policy’s impact on SBER.

Learn to differentiate between QI activities and the types of activities that constitute regulated research involving human subjects.

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These guides provide resources and guidance for developing and facilitating in-person or virtual RCR training sessions.

Explores the concept of race in clinical research and important ethical and regulatory questions.

Discusses ways to improve diversity and equity among clinical trial participants.

Understand factors that may determine participant payment decisions.

Discusses why technology-based expertise is critical to human subject protections and how to add IT insights to IRB review.

An overview of connected and automated vehicles (CAVs) and the associated privacy and ethical challenges.

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Learn about QA/QI programs, how to conduct an internal audit, and strategies for using the findings.

Reviews how to properly conduct an accident investigation, including identifying the root cause and implementing corrective act...

Describes regulatory requirements for a CAPA system in the biotech industry.

Provides an overview of the U.S. DOE’s interim policy on conflicts of interest.

QA/QI professionals can learn to audit ceded studies for single IRB (sIRB) review.

This course covers the fundamental safety practices for working with hazardous chemicals in the laboratory.

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Provides best practices for instructors on how to navigate the current challenges of online and hybrid learning while actively engaging with learners throughout the entire educational process.

Helps develop leadership skills to meet today’s changing, diverse, and dynamic environments.

Discusses the importance of CRA soft skills in building productive relationships with sites and sponsors.

Explores the role of predictive analytics in higher ed, its ethical challenges, and ways to implement it ethically.

Learn how to communicate research results to the public and policymakers using different models and strategies.

Provides learners with practical tips to make ADA, Section 504, and accommodations in the 21st century more accessible and equi...

Browse all of the courses and series available from CITI Program.

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.

Tech Software a leading provider of SaaS compliance solutions for higher-education, academic medical centers, hospitals, government and biotech companies.

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.