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Co-Authored-By: Claude Opus 4.8 <noreply@anthropic.com>
2026-07-06 10:51:44 -04:00

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LegalText 21 U.S.C. § 360a Clinical trial guidance for antibiotic drugs us united_states_code code_section 21 FOOD AND DRUGS 9 FEDERAL FOOD, DRUG, AND COSMETIC ACT 360a 21 U.S.C. § 360a current 119-100 2026-06-26 official https://uscode.house.gov/download/releasepoints/us/pl/119/100/xml_usc21@119-100.zip /us/usc/t21/s360a data/legal/raw/us/code/title-21/usc21.xml a7c2b71876fc914bdddb9d8ea97f1994bd115f6089fcee560a76bf1f7841ad38 3dbd7a61c8616baefb8459bd8dac3b93242106deb416308c8d4dd5a9143176d1 e5a426b40bb338203c7b2dda3cd5f446eecbc125cb8621ec45ba4ddc13f34f3a 2026-07-04 official
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21 U.S.C. § 360a - Clinical trial guidance for antibiotic drugs

Text

(a) In general Not later than 1 year after September 27, 2007, the Secretary shall issue guidance for the conduct of clinical trials with respect to antibiotic drugs, including antimicrobials to treat acute bacterial sinusitis, acute bacterial otitis media, and acute bacterial exacerbation of chronic bronchitis. Such guidance shall indicate the appropriate models and valid surrogate markers.

(b) Review Not later than 5 years after September 27, 2007, the Secretary shall review and update the guidance described under subsection (a) to reflect developments in scientific and medical information and technology.

(June 25, 1938, ch. 675, § 511, as added Pub. L. 11085, title IX, § 911, Sept. 27, 2007, 121 Stat. 951.)

Notes

Editorial Notes

Prior ProvisionsA prior section 360a, act June 25, 1938, ch. 675, § 511, as added July 15, 1965, Pub. L. 8974, § 3(b), 79 Stat. 227; amended Oct. 24, 1968, Pub. L. 90639, § 2(a), 82 Stat. 1361, regulated the manufacture, compounding, and processing of depressant and stimulant drugs and their sale, delivery, disposal, possession, and recordkeeping activities connected therewith, prior to repeal by Pub. L. 91513, title II, §§ 701(a), 704, Oct. 27, 1970, 84 Stat. 1281, 1284, effective on the first day of the seventh calendar month that began after Oct. 26, 1970.