# Guidance for Industry: Questions and Answers Regarding Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/guidance-for-industry-questions-and-answers-regarding-adverse-event-reporting-and-recordkeeping-for-dietary-supplements-as-required-by-the-dietary-supplement-and-nonprescription-drug-consumer-protection-act/8c5632c8-16c0-4996-aa58-70c9a556d69d

> FDA guidance document: Guidance for Industry: Questions and Answers Regarding Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act. Issue date: September 01, 2013. Get complete insights and analysis.

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## Details

- Title: Guidance for Industry: Questions and Answers Regarding Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act
- Communication Type: Guidance Document
- Product Type: dietary_supplements
- Office Name: Human Foods Program
- Office URL: /offices/human-foods-program/8bff4a0b-7bed-449c-b67b-56a83c96a324
- Issue Date: 2013-09-01
- Last Changed: 2025-02-05
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2007-D-0372">FDA-2007-D-0372</a>

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