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U.S Food and Drug Administration


Dietary Supplement Usage Up Dramatically During Pandemic, New Ipsos-CRN Survey Shows

by Shari Barbanel | August 26, 2020

The Council for Responsible Nutrition (CRN) has issued results of a COVID-19-focused consumer survey that discovered more than two in five (43 percent) of dietary supplement users have changed their supplement routines since the start of the pandemic. Among those who altered their regimens due to COVID-19, 91 percent report increasing their supplement intake which ...

USP Offers Hand Sanitizer Toolkit in Response to the COVID-19 Pandemic

by Shari Barbanel | April 13, 2020

The U.S. Pharmacopeia (USP) is offering an online toolkit with guidelines from major public health organizations on compounding alcohol-based hand sanitizers and the preparation of hand sanitizers by manufacturers, pharmacies and other facilities. The toolkit was developed to help organizations meet the demand for these products, as shortages of commercially manufactured sanitizers have occurred. The toolkit includes important ...

FDA Fails to Deliver Congressionally Mandated Report on CBD Regulations

by Shari Barbanel | February 26, 2020

The U.S. Food and Drug Administration (FDA) failed to meet its deadline to provide a Congressionally mandated report on how it plans to regulate CBD. Congress instructed the FDA in last year’s spending bill to adopt an enforcement discretion policy within 120 days and provide an update of its progress after 60 days. The agency’s first report ...

NPA Urges Health Care Professionals to Report Adverse Events for Dietary Supplements

by Shari Barbanel | January 16, 2020

In a letter to leading medical societies, the Natural Products Association (NPA) is urging that health care professionals make recommendations for reporting adverse events for dietary supplements. Manufacturers of dietary supplements are required to submit all information pertaining to adverse events associated with their products to the FDA (U.S. Food and Drug Administration). “Adverse events ...

Senate Confirms Hahn as FDA Commissioner

by Shari Barbanel | December 16, 2019

In a 72-18 Senate vote, Stephen Hahn, MD, FASTRO was confirmed as the new head of the U.S. Food and Drug Administration (FDA), taking charge at a regulatory agency that oversees products ranging from complex cancer drugs, to food, cosmetics, tobacco and CBD. “We look forward to working with Dr. Hahn and his staff to ...

President Trump Nominates Stephen Hahn as FDA Commissioner

by Shari Barbanel | November 6, 2019

According to Politico, President Donald Trump announced last week that he will nominate Stephen Hahn, MD, FASTRO, a cancer specialist and hospital administrator, to lead the FDA (U.S. Food and Drug Administration). Trump had been rumored to make this selection for several months. If confirmed by the Senate, the top FDA post would mark Hahn’s first ...

House of Representatives Instructs FDA to Regulate CBD

by Shari Barbanel | July 16, 2019

Legislation passed the House of Representatives on June 25 that would appropriate $100,000 for the U.S. Food and Drug Administration (FDA) to perform a Health Hazard Evaluation (HHE) and set a safe level of CBD for consumers to use each day. The process would follow the same precedent as red yeast rice, which allows a natural product to ...

FDA Holds CBD Public Hearing

by Shari Barbanel | June 3, 2019

The U.S. Food and Drug Administration (FDA) held a public hearing on cannabidiol, also known as CBD, at its Silver Spring, MD headquarters on Friday, May 31. The New York Times(NYT), called the hearing “the hottest ticket in the capital.” More than 400 applicants, from the U.S. Hemp Roundtable to blue chip law firms, had ...

New Farm Bill is Imminent as it Passes House and Senate

by Shari Barbanel | December 12, 2018

On the evening of Dec. 10, the 2018 Farm Bill House/Senate Conference Committee released its Conference Report. The 807-page document is nearly half a foot tall. Hemp is discussed in only a few handfuls of pages. As of press time, the Senate passed the bill on Dec. 11 by a vote of 87 to 13; ...

FDA Announces New Final Guidances on Revised Nutrition Labeling Requirements

by Shari Barbanel | November 5, 2018

On November 2, the U.S. Food and Drug Administration (FDA) announced two new final guidances to help companies revise nutrition labels for conventional foods and dietary supplements to comply with the new regulations. One document deals with the definition of a single-serving container, reference amounts customarily consumed, which are used by companies to determine serving ...

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