Modernizing the Regulatory Framework for Dietary Supplements: A Position Paper From the American College of Physicians.

Strengthening FDA oversight of dietary supplements could reduce adulterated and mislabeled products entering the U.S. market, protecting public health.

• Why it matters: Current regulations treat dietary supplements as foods, leaving them unreviewed by the FDA and increasing risks of unsafe products reaching consumers. Addressing this gap is crucial for safeguarding public health and ensuring product safety.
• What they did: The American College of Physicians proposes policy changes to enhance the FDA's regulatory authority before and after market entry, standardize terminology and data sharing, and improve healthcare practices related to supplement use.
• The result: Implementing these recommendations could lead to safer dietary supplements, better regulatory oversight, and improved patient care for those using these products.