The Food and Drug Administration oversees a broad range of medical and consumer products. In fact, the agency estimates that the items it regulates account for 20 cents of each dollar Americans spend.

The health care products project worked to advance policies that would effectively protect consumers from dangerous products and reduce safety risks associated with new innovations in the marketplace. Its efforts focused on diagnostic tests, dietary supplements, over-the-counter drugs, and regenerative medicine. The project concluded in 2022.

National Cancer Institute
National Cancer Institute
Report

Lab-Developed Tests in the In Vitro Diagnostics Market

Quick View
Report

In vitro diagnostic (IVD) tests—which use blood, saliva, and other human samples to detect the presence or risk of certain diseases—are a pillar of modern medicine.

How FDA Regulates Artificial Intelligence in  Medical Products
How FDA Regulates Artificial Intelligence in  Medical Products
Issue Brief

How FDA Regulates Artificial Intelligence in Medical Products

Quick View
Issue Brief

Health care organizations are using artificial intelligence (AI)—which the U.S. Food and Drug Administration defines as “the science and engineering of making intelligent machines”—for a growing range of clinical, administrative, and research purposes. This AI software can, for example, help health care providers diagnose diseases, monitor patients’ health, or assist with rote functions such as scheduling patients.

A nurse pushes a wheeled stretcher in the hallway of a hospital
A nurse pushes a wheeled stretcher in the hallway of a hospital
Issue Brief

Harms Linked to Unapproved Stem Cell Interventions

Quick View
Issue Brief

Stem cell products and other regenerative therapies have significant potential to treat traumatic injuries and serious diseases. Although some have earned approval from the Food and Drug Administration, most have not, and many of these unapproved interventions have led to life-threatening infections, chronic pain, and even death.

Getty Images
Getty Images
Fact Sheet

Americans Support The FDA Tracking Supplement Ingredients

Quick View
Fact Sheet

Americans Support The FDA Tracking Supplement Ingredients

Four in 5 American adults report having used supplements, products that can include vitamins, minerals, plant and animal extracts, hormones, and amino acids. The Food and Drug Administration (FDA) oversees the safety of supplements, and nearly all adults say the agency should have this responsibility.

Our Work

This video is hosted by YouTube. In order to view it, you must consent to the use of “Marketing Cookies” by updating your preferences in the Cookie Settings link below. View on YouTube

This video is hosted by YouTube. In order to view it, you must consent to the use of “Marketing Cookies” by updating your preferences in the Cookie Settings link below. View on YouTube

Can Dietary Supplements Harm You?