FEDERAL · 42 U.S.C. · Chapter 6A

Manufacturer recordkeeping and reporting

Current through Pub. L. 119-102
Title 42The Public Health and Welfare·Ch. 6A — PUBLIC HEALTH SERVICE·Subch. XIX·Pt. 2
(a)General rule Each vaccine manufacturer of a vaccine set forth in the Vaccine Injury Table or any other vaccine the administration of which is mandated by the law or regulations of any State, shall, with respect to each batch, lot, or other quantity manufactured or licensed after December 22, 1987—
(1)prepare and maintain records documenting the history of the manufacturing, processing, testing, repooling, and reworking of each batch, lot, or other quantity of such vaccine, including the identification of any significant problems encountered in the production, testing, or handling of such batch, lot, or other quantity,
(2)if a safety test on such batch, lot, or other quantity indicates a potential imminent or substantial public health hazard is presented, report to the Secretary withi

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42 U.S.C. § 300aa–28 (Manufacturer recordkeeping and reporting) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

Source Credit

History

(July 1, 1944, ch. 373, title XXI, §2128, as added Pub. L. 99–660, title III, §311(a), Nov. 14, 1986, 100 Stat. 3777; amended Pub. L. 100–203, title IV, §4302(b)(1), Dec. 22, 1987, 101 Stat. 1330–221.)

Editorial Notes

Editorial Notes

Codification
In subsec. (a), "December 22, 1987" substituted for "the effective date of this subpart" on authority of section 323 of Pub. L. 99–660, as amended, set out as an Effective Date note under section 300aa–1 of this title.

Amendments
1987—Subsec. (a). Pub. L. 100–203 substituted "effective date of this subpart" for "effective date of this part".