How does the FDA ensure the safety of dietary supplements?
Dietary supplements are regulated differently from drugs. The Dietary Supplement Health and Education Act grants the FDA authority to oversee the safety of these products. Manufacturers must ensure that their supplements are safe and properly labeled. The FDA monitors adverse event reports and can take enforcement actions against unsafe supplements, including recalls and warning letters.
In conclusion, the FDA's role in toxicology is multifaceted, encompassing the evaluation, regulation, and monitoring of substances across a wide range of products. By establishing stringent safety standards and conducting thorough assessments, the FDA aims to protect public health and maintain consumer confidence in the products available in the United States.
