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FDA Request For Clarifying DSHEA, Like Mandatory Listing, Splits US Supplement Industry Groups

 
• By Malcolm Spicer

Already differing on supporting FDA suggestion for mandatory annual registration of each VMS product sold in US, consumer health industry stakeholders’ schism now extends to agency suggestion that Congress clarify its regulatory authority over supplement manufacturing and marketing.

• Source: Alamy

The consumer health products industry hasn’t been unanimous about agreeing with the Food and Drug Administration on imposing mandatory annual registration of each dietary supplement product sold in the US.

The schism also now extends to the agency’s suggestion to Congress included in the justification document for its fiscal year...

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US FDA Extracts More Evidence To Ban Kratom

 
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Cloudy Tariff Conditions Expected To Linger In US

 
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More from Policy & Regulation

US FDA Extracts More Evidence To Ban Kratom

 
• By Malcolm Spicer

Recent warning letters to seven companies marketing products with kratom extract known as 7-OH are FDA’s first in three years referencing unlawful products containing kratom and the first of all its kratom-related warnings to reference extracts from the botanical.

HHS Wants Employees (And Public?) To Report Diversity, Equity And Inclusion Discrimination

 
• By Sue Sutter

A survey asks FDA staff to disclose whether DEI policies caused discrimination or resulted in disciplinary action against career employees over the past five years, but uses a web form that the general public also can access.

Cloudy Tariff Conditions Expected To Linger In US

 
• By Malcolm Spicer

White House announces president extends deadline he set in April for other countries to make new tariff deals from July 9 to Aug. 1, when the administration will start sending letters warning other countries that higher tariffs could take effect.