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# FDA Public Meetings on e-Adverse Event Reports
- URL: https://www.fdaweb.com/fda-public-meetings-on-e-adverse-event-reports/
- Published: 2018-11-15T12:00:00.000Z
- Updated: 2026-09-15T00:45:06.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5142829

*Federal Register* notice: FDA has announced three public meetings entitled “Electronic Submission of Adverse Event Reports to FDA Adverse Event Reporting System (FAERS) Using International Council for Harmonization (ICH) E2B(R3) Standards.” The meetings are intended to provide the pharmaceutical industry and other interested parties with information on the plans, progress, and technical specifications to upgrade electronic submission standards for drug, biological, and drug/biologic-led combination products for the premarket and postmarket safety surveillance programs managed by CDER and CBER. To view the notice, click [here](https://s3.amazonaws.com/public-inspection.federalregister.gov/2018-25063.pdf?ref=fdaweb.com).