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Industry Responds to Dr. Marty Makary’s Nomination as FDA Commissioner

by Eric Munson | December 3, 2024

On Nov. 22, President-elect Donald Trump nominated Dr. Marty Makary as commissioner for the U.S. Food and Drug Administration (FDA). He would succeed outgoing FDA Commissioner Robert Califf. Makary is a surgical oncologist at Johns Hopkins Hospital in Baltimore, MD. He is also a professor at the Johns Hopkins School of Medicine, a researcher, an ...

Industry Responds to RFK Jr.’s Nomination as HHS Director

by Eric Munson | November 18, 2024

On Nov. 14, President-elect Donald Trump nominated environmental attorney Robert F. Kennedy Jr. (RFK) as director of the Department of Health and Human Services (HHS). After ending his own presidential campaign, Kennedy endorsed Trump and has since launched “Make America Healthy Again,” a campaign that “prioritizes regenerative agriculture, protects natural resources and removes harmful toxins ...

The Supplement OWL Takes Flight

by Shari Barbanel | April 27, 2017

One year after the project was formally announced, the Supplement OWL (Online Wellness Library) became a reality, as the online product registry is now live. Serving as a resource for regulators, retailers, and industry, the OWL is an industry-wide, self-regulatory initiative that will help create a rich and more complete picture of the marketplace, and ...

Industry Calls on FDA to Create Separate Office of Dietary Supplements

by Shari Barbanel | September 9, 2015

The Natural Products Association (NPA) along with the Council for Responsible Nutrition (CRN), Consumer Healthcare Products Association (CHPA) and the United Natural Products Alliance (UNPA) have called on the U.S. Food and Drug Administration (FDA) to elevate their Division of Dietary Supplement Programs (DDSP) in the Center for Food Safety and Applied Nutrition to an ...

Focus On Food Safety

by Kate Quackenbush | April 1, 2012

NIE discusses the implications posed by FSMA with industry representatives, and their work to meet the challenges head on.In 2007, the U.S. Food and Drug Administration (FDA) published a “Final Rule,” establishing FDA regulations, which require current good manufacturing practices (cGMP) for dietary supplements (21 CFR 111). The final rule addresses in particular the identity, ...

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