Clinical trial guidance for antibiotic drugs

  1. Law
  2. USC 21
  3. Food And Drugs
  4. FEDERAL FOOD, DRUG, AND COSMETIC ACT
  5. DRUGS AND DEVICES
  6. Drugs and Devices
  7. Clinical trial guidance for antibiotic drugs

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§360a. Clinical trial guidance for antibiotic drugs

(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. 110–85, title IX, §911, Sept. 27, 2007, 121 Stat. 951 .)

Prior Provisions

A prior section 360a, act June 25, 1938, ch. 675, §511, as added July 15, 1965, Pub. L. 89–74, §3(b), 79 Stat. 227 ; amended Oct. 24, 1968, Pub. L. 90–639, §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. 91–513, 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.


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