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FDA's Cosmetic AE Data Begs Question: What If Reporting Were Mandatory?

 
• By Ryan Nelson

Infographic: According to FDA data, cosmetic-related AE reports in 2015 more than tripled what they were in 2009, but consumers still do the bulk of the reporting themselves. Proposed federal bills to update cosmetics oversight would require companies to report serious adverse events, which could propel numbers upward while providing FDA with greater insight into the marketplace.

Cosmetics reform bills under consideration in the US Congress invite speculation as to whether the marketplace picture would change dramatically if adverse-event reporting were required of companies.

Nakissa Sadrieh, director of the cosmetics program within FDA's Office of Cosmetics and Colors, presented data on cosmetic AE reporting...

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More from Policy & Regulation

MoCRA Implementation Delay Creates More Legal Exposure For Stakeholders – Attorney

 
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