The US Food and Drug Administration’s recently appointed acting food safety chief is heading a program introduced as new in October but is greeted by the same problems in the dietary supplement market the agency’s found for decades, products spiked with undisclosed drugs.
Old Problem Of Drugs In Supplements Welcomes US FDA’s Acting Food Chief To New Program
Kyle Diamantas was a partner with the Jones Day firm when he was tabbed as acting deputy commissioner to lead the FDA’s Human Foods Program, established in the agency’s reorganization which became effective in October.
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Kyle Diamantas was a partner with the Jones Day firm when he was tabbed as acting deputy commissioner to lead the FDA’s Human Foods Program, established in the agency’s reorganization which became effective in October.
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Streamlined process for reporting problems is key piece of “unified Human Foods Program” which officially launched on 1 October, as Commissioner Robert Califf says, “a new model for field operations and other modernization efforts.”
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Brands also making market moves as lawmakers consider legislation instructing Transportation Security Administration to provide guidance to minimize risk for contamination of baby formula and related pediatric nutritional products.
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Green Pharmaceuticals’ SnoreStop Nasal Spray, previously marketed as “NasoSpray,” still is available even though agency officials on multiple occasions for a month recommended a recall after an April inspection found “gross microbial contamination” in one lot.
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Parking and security at the FDA’s White Oak headquarters were strained from the influx of employees who had to report to work in person on 17 March.