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# Info Collection Extension for e-Adverse Event Reports
- URL: https://www.fdaweb.com/info-collection-extension-for-e-adverse-event-reports/
- Published: 2018-12-03T12:00:00.000Z
- Updated: 2026-09-15T00:48:14.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5142943

*Federal Register* notice: FDA is seeking comments on an information collection extension entitled “FDA Adverse Event Reports; Electronic Submissions — 21 CFR 310.305, 314.80, 314.98, 314.540, 514.80, 600.80, 1271.350, and Part 803” (OMB Control Number 0910-0645). To view the notice, click [here](https://www.gpo.gov/fdsys/pkg/FR-2018-11-30/pdf/2018-26031.pdf?ref=fdaweb.com).