Title 21 › Chapter CHAPTER 9— - FEDERAL FOOD, DRUG, AND COSMETIC ACT › Subchapter SUBCHAPTER V— - DRUGS AND DEVICES › Part Part E— - General Provisions Relating to Drugs and Devices › § 360bbb–8b
The Secretary must accept clinical trial data from studies done outside the United States, including the European Union, if the applicant shows the data meet the applicable U.S. standards to support approval, licensure, or clearance of a drug, biological product, or device. If the Secretary decides the outside data are not adequate for a decision, the Secretary must give the application sponsor written notice and explain the reasons.
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Food and Drugs — Source: USLM XML via OLRC
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Citation
21 U.S.C. § 360bbb–8b
Title 21 — Food and Drugs
Last Updated
Apr 6, 2026
Release point: 119-73