{"id":86050,"date":"2025-07-29T08:00:54","date_gmt":"2025-07-29T06:00:54","guid":{"rendered":"https:\/\/www.veeva.com\/eu\/?post_type=resources&#038;p=86050"},"modified":"2026-01-27T15:10:38","modified_gmt":"2026-01-27T14:10:38","slug":"submitting-icsrs-using-fda-e2br3-standard","status":"publish","type":"resources","link":"https:\/\/www.veeva.com\/eu\/resources\/submitting-icsrs-using-fda-e2br3-standard\/","title":{"rendered":"Submitting ICSRs Using FDA E2B(R3) Standard"},"content":{"rendered":"<p>Electronically submit premarketing and postmarketing Individual Case Safety Reports (ICSRs) to the FDA Adverse Event Reporting System (FAERS) database using the E2B(R3) standard.<\/p>\n<p>To find out more, visit <a href=\"\/eu\/products\/veeva-safety\/\">Veeva Safety<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Electronically submit premarketing and postmarketing Individual Case Safety Reports (ICSRs) to the FDA Adverse Event Reporting System (FAERS) database using the E2B(R3) 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