Legalize59765 laws
59765 laws
- § 360ddd–1. Regulation of medical gases
- § 360ddd–2. Inapplicability of drug fees to designated medical gases
- § 360e. Premarket approval
- §§ 1503 to 1505. Repealed. [Aug. 26, 1954, ch. 937](/us/act/1954-08-26/ch937), title V, § 542(a)(4), (10), [68 Stat. 861](/us/stat/68/861)
- § 360ee. Grants and contracts for development of drugs for rare diseases and conditions
- § 360eee. Definitions
- § 360eee–1. Requirements
- § 360eee–2. National standards for prescription drug wholesale distributors
- § 360eee–3. National standards for third-party logistics providers
- § 360eee–4. Uniform national policy
- § 360ee–1. FDA rare neurodegenerative disease grant program
- § 360e–1. Pediatric uses of devices
- § 360e–3. Breakthrough devices
- § 360ff. Priority review to encourage treatments for rare pediatric diseases
- § 360fff. Definitions
- § 360fff–1. Submission of requests
- § 360fff–2. Eligibility determinations; data submission; filing
- § 360fff–3. GRASE determination
- § 360fff–4. Guidance; other provisions
- § 360fff–5. Repealed. [Pub. L. 116–136, div. A, title III, § 3854(b)(5)](/us/pl/116/136/dA/tIII/s3854/b/5), Mar. 27, 2020, [134 Stat. 456](/us/stat/134/456)
- § 360fff–6. Non-sunscreen time and extent applications
- § 360fff–7. Report
- § 360fff–8. Sunset
- § 360ff–1. Targeted drugs for rare diseases
- § 360g. Judicial review
- § 360g–1. Agency documentation and review of significant decisions regarding devices
- § 360g–2. Third party data transparency
- § 360h. Notification and other remedies
- § 360hh. Definitions
- § 360h–1. Program to improve the device recall system
- § 360i. Records and reports on devices
- § 360ii. Program of control
- § 1506. Repealed. [Oct. 10, 1951, ch. 479](/us/act/1951-10-10/ch479), title V, § 503(b)(1), as added [June 20, 1952, ch. 449, § 7(c)](/us/act/1952-06-20/ch449/s7/c), [66 Stat. 144](/us/stat/66/144)
- § 360j. General provisions respecting control of devices intended for human use
- § 360jj. Studies by Secretary
- § 360kk. Performance standards for electronic products
- § 360l. Postmarket surveillance
- § 360ll. Notification of defects in and repair or replacement of electronic products
- §§ 1507 to 1513. Repealed. [Aug. 26, 1954, ch. 937](/us/act/1954-08-26/ch937), title V, § 542(a)(4), (6), (9)–(11), [68 Stat. 861](/us/stat/68/861)
- § 360m. Accredited persons
- § 360mm. Imports
- § 360n. Priority review to encourage treatments for tropical diseases
- § 360nn. Inspection, records, and reports
- § 360n–1. Priority review for qualified infectious disease products
- § 360n–2. Ensuring cybersecurity of devices
- § 360oo. Prohibited acts
- § 360pp. Enforcement
- § 360qq. Repealed. [Pub. L. 105–362, title VI, § 601(a)(2)(A)](/us/pl/105/362/tVI/s601/a/2/A), Nov. 10, 1998, [112 Stat. 3285](/us/stat/112/3285)
- § 360rr. Federal-State cooperation
- § 360ss. State standards