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Potential For US Requiring Supplement Registration Underscored During FDA’s Hiatus From Inspections

 
• By Eileen Francis

FDA’s pause in facility inspections could prompt draft legislation for mandatory supplement product registration. It told industry groups it’s working on language for legislation to give it a better handle on products in the market and facilities with problems, says CRN head Steve Mister.

mandatory word in a dictionary. mandatory concept.

The potential for adulterated dietary supplements to reach the US market during the four months the Food and Drug Administration paused its facility inspections highlights the need for mandatory product listing and could prompt introduction of legislation to impose the requirement.

FDA has informed supplement industry stakeholders it is working on language for a proposal to submit to members of Congress that would codify a mandatory listing process, says

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Four months into session, no bills have been introduced in Congress to authorize FDA to establish a regulatory pathway for the lawful use of hemp ingredients in products other than drugs or propose some other solution to the federal conundrum present since lawmakers in 2018 de-scheduled hemp.

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• By David Ridley

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More from Policy & Regulation

Third-Party ‘Testing, Inspection and Certification’ Cleaning Up Amazon Supplement Market

 
• By Malcolm Spicer

Three FDA warnings related to supplement manufacturing, labeling or marketing submitted to Amazon or companies selling vitamin, mineral or supplement products on its e-commerce platform since April 2024.

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• By Malcolm Spicer

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