Title 21 › Chapter 9— FEDERAL FOOD, DRUG, AND COSMETIC ACT › Subchapter V— DRUGS AND DEVICES › Part E— General Provisions Relating to Drugs and Devices › § 360bbb–1
The Secretary must make rules allowing sponsors, applicants, or manufacturers to seek review of scientific disputes about requirements for drugs or devices under this Act or section 351 when no review right exists; reviews can use a panel under 355(n) or a committee under 360e(g)(2)(B), must be timely, and the rules were due within 1 year after November 21, 1997.
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Food and Drugs, Source: USLM XML via OLRC
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21 U.S.C. § 360bbb–1
Title 21, Food and Drugs
Last Updated
Apr 5, 2026
Release point: 119-73not60