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  1. Focus Areas of Regulatory Science Report

Medical Product Development Tools


A collage of photos showing a teenage girl entering an MRI machine, a gloved hand inserting a syringe into a vaccine vial, and a pile of prescription pill bottles.

Publicly available, FDA-qualified, medical product development tools facilitate industry’s ability to harness innovative science and technology. These tools, methods, and models are used to reduce the time, complexity, or cost of developing FDA-regulated products, while increasing the reliability and robustness of the results used to support product development.




Minority Health and Health Equity Women’s Health Maternal Health Pediatric Health
Oncology Rare Diseases One Health Initiative  



Research Capabilities, Tools, and Resources

Research Management and Collaborations Technology Transfer and Public-Private Partnerships Physical Standards and Reference Materials Intramural Grant Programs Extramural Funding Mechanisms

Scientific Education, Training, and Communication

Fellowship and Training Opportunities Professional Development and Continuing Education Communication and External Meetings


Facilities and Shared Resources Safety and Compliance



Office of the Chief Scientist

Office of Regulatory Science and Innovation

Contact Us: FARS@fda.hhs.gov


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