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21 CFR 822.2

§ 822.2 What is the purpose of this part?

United States · 21 CFR — Food and Drugs · Status: effective

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21 CFR 822.2, § 822.2 What is the purpose of this part?, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/88921
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Full text

The purpose of this part is to implement our postmarket surveillance authority to maximize the likelihood that postmarket surveillance plans will result in the collection of useful data. These data can reveal unforeseen adverse events, the actual rate of anticipated adverse events, or other information necessary to protect the public health.

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.