# 21 U.S.C. § 360jj: Studies by Secretary

> Federal · Statutes · In force

URL: https://www.frixlaw.com/law-library/statutes/usc_t21_s360jj

## Section

- **Citation:** 21 U.S.C. § 360jj
- **Heading:** Studies by Secretary
- **Jurisdiction:** Federal
- **Kind:** Statutes
- **Status:** In force
- **Text as of:** April 17, 2026
- **Source:** Publisher's official text
- **Location:** Title 21—FOOD AND DRUGS > CHAPTER 9—FEDERAL FOOD, DRUG, AND COSMETIC ACT > SUBCHAPTER V—DRUGS AND DEVICES > Part C—Electronic Product Radiation Control

## Text

control of health hazards from radioactive materials other than materials regulated under the Atomic Energy Act of 1954 [ 42 U.S.C. 2011 et seq.];

( June 25, 1938, ch. 675, § 533 , formerly act July 1, 1944, ch. 373, title III, § 533 , formerly § 357, as added Pub. L. 90–602, § 2(3) , Oct. 18, 1968 , 82 Stat. 1176 ; renumbered § 533 and amended Pub. L. 101–629, § 19(a)(1)(B) , (3), (4), Nov. 28, 1990 , 104 Stat. 4529 , 4530; Pub. L. 103–80, § 4(a)(2) , Aug. 13, 1993 , 107 Stat. 779 .)

## Nearby sections

- [21 U.S.C. § 351 Adulterated drugs and devices](https://www.frixlaw.com/law-library/statutes/usc_t21_s351.md)
- [21 U.S.C. § 352 Misbranded drugs and devices](https://www.frixlaw.com/law-library/statutes/usc_t21_s352.md)
- [21 U.S.C. § 353 Exemptions and consideration for certain drugs, devices, and biological products](https://www.frixlaw.com/law-library/statutes/usc_t21_s353.md)
- [21 U.S.C. § 353a Pharmacy compounding](https://www.frixlaw.com/law-library/statutes/usc_t21_s353a.md)
- [21 U.S.C. § 353a–1 Enhanced communication](https://www.frixlaw.com/law-library/statutes/usc_t21_s353a%E2%80%931.md)
- [21 U.S.C. § 353b Outsourcing facilities](https://www.frixlaw.com/law-library/statutes/usc_t21_s353b.md)
- [21 U.S.C. § 353c Prereview of television advertisements](https://www.frixlaw.com/law-library/statutes/usc_t21_s353c.md)
- [21 U.S.C. § 353d Process to update labeling for certain generic drugs](https://www.frixlaw.com/law-library/statutes/usc_t21_s353d.md)
- [21 U.S.C. § 354 Veterinary feed directive drugs](https://www.frixlaw.com/law-library/statutes/usc_t21_s354.md)
- [21 U.S.C. § 355 New drugs](https://www.frixlaw.com/law-library/statutes/usc_t21_s355.md)
- [21 U.S.C. § 355–1 Risk evaluation and mitigation strategies](https://www.frixlaw.com/law-library/statutes/usc_t21_s355%E2%80%931.md)
- [21 U.S.C. § 355–2 Actions for delays of generic drugs and biosimilar biological products](https://www.frixlaw.com/law-library/statutes/usc_t21_s355%E2%80%932.md)
- [21 U.S.C. § 355a Pediatric studies of drugs](https://www.frixlaw.com/law-library/statutes/usc_t21_s355a.md)
- [21 U.S.C. § 355b Adverse-event reporting](https://www.frixlaw.com/law-library/statutes/usc_t21_s355b.md)

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Source: Frix Law Library, https://www.frixlaw.com/law-library/statutes/usc_t21_s360jj. Check the current official text before relying on it. Not legal advice.