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# 2 Meetings on Adverse Event Reporting
- URL: https://www.fdaweb.com/2-meetings-on-adverse-event-reporting/
- Published: 2023-02-16T12:00:00.000Z
- Updated: 2026-09-14T18:16:22.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5153795

*Federal Register* notice: FDA is announcing two 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.” They are intended to provide the pharmaceutical industry and other interested parties with updated information on the plans, progress, and technical specifications to upgrade electronic submission standards for drug, biological product, and drug- or biologic-led combination products in the premarket and postmarket safety surveillance programs managed by the CDER/CBER. To view the notice, click [here](https://public-inspection.federalregister.gov/2023-03372.pdf?ref=fdaweb.com).