21 CFR 803.11
§ 803.11 What form should I use to submit reports of individual adverse events and where do I obtain these forms?
United States · 21 CFR — Food and Drugs · Status: effective
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- Citation
- 21 CFR 803.11, § 803.11 What form should I use to submit reports of individual adverse events and where do I obtain these forms?, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/88702
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Full text
(a) If you are a manufacturer or importer, you must submit reports of individual adverse events to FDA in an electronic format in accordance with § 803.12(a) and § 803.20, unless granted an exemption under § 803.19.
(b) Importer reports submitted to device manufacturers may be in paper format or an electronic format that includes all required data fields to ensure that the manufacturer has all required information.
(c) If you are a user facility, you must submit reports of individual adverse events in accordance with § 803.12(b) and § 803.20.
(d) Form FDA 3500A is available on the internet at https://www.accessdata.fda.gov/scripts/medwatch/index.cfm.
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.