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.

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

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.

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

This course provides training on working with birds in research settings.

A condensed and combined single-module course based on the NSF Research Security Training.

This course provides an overview of export compliance regulations along with information specifically tailored for certain roles and responsibilities.

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

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

This course provides training on working with insects in research settings.

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

An overview of detection and remedies for academic integrity violations.

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

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

Covers the principles, governance approaches, practices, and tools for responsible artificial intelligence (AI) development and use.

This course addresses ways to create and maintain healthy workplace environments in various research settings.

This course provides foundational training on conflicts of interest for healthcare professionals.

An overview of Medicare for healthcare operations, covering Parts A, B, C, and D as well as key aspects of its administration, audits, and oversight.

A review of HIPAA’s HITECH Act of 2009 geared toward business associates, vendors, and others subject to HIPAA.

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

Covers the regulatory aspects related to SaMD and CDSS when conducting clinical investigations and other considerations.

Provides fundamental knowledge of clinical trial regulatory affairs.

Provides foundational training on conflict of interest and commitment requirements set forth by various federal agencies.

An introduction to SBIR-STTR programs.

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

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

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

Describes field navigation and discusses the map, compass, and GPS tools, and skills to plan a route and what to do if you get lost.

Empower yourself to effectively intervene and support others in critical situations with our comprehensive Bystander Training course.

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.