fda
FDA to Hold Public Meeting on Responsible Innovation in Dietary Supplements
The U.S. Food and Drug Administration (FDA) recently announced a May 16 public meeting entitled “Responsible Innovation in Dietary Supplements.” On Feb. 11, 2019, the FDA announced new efforts to strengthen the regulation of dietary supplements by modernizing and reforming its oversight. The purpose of the public meeting is to give interested parties an opportunity to present ...
Gottlieb Discusses CBD at House Appropriations Committee Hearing
On April 3, former FDA (U.S. Food and Drug Administration) Commissioner Scott Gottlieb, MD, provided insights into the agency’s approach to products that contain cannabidiol (CBD) during a House Appropriations Committee hearing on FDA funding for 2020. In two exchanges with Rep. Andy Harris (R-MD), Gottlieb reiterated that the agency considers most CBD products on ...
AHPA Adopts Policy on Items Containing Hemp/CBD
The American Herbal Products Association (AHPA) has adopted a new Guidance Policy for dietary supplement and food products that contain hemp and hemp-derived cannabidiol (CBD) to help ensure the industry complies with existing regulations. The guidance policy was developed to encourage industry to be mindful of the federal regulations that apply to these product categories, notwithstanding FDA ...
FDA Public Meeting on Cannabis to be Held in May
On May 31, FDA (U.S. Food and Drug Administration) will hold a public meeting to “obtain scientific data and information about the safety, manufacturing, product quality, marketing, labeling, and sale of products containing cannabis or cannabis-derived compounds,” as noted in the Federal Register. In a statement, outgoing FDA Commissioner Scott Gottlieb, MD noted that “the ...
Ned Sharpless Named Acting FDA Commissioner
Following the resignation of Scott Gottlieb, Norman E. “Ned” Sharpless, MD, has been named the acting commissioner of the FDA (U.S. Food and Drug Administration) by Alex Azar, the Health and Human Services (HHS) secretary, effective April 2019. “Dr. Sharpless’ deep scientific background and expertise will make him a strong leader for FDA,” said Azar ...
FDA Commissioner Gottlieb Resigning
U.S. Food and Drug Administration (FDA) chief Scott Gottlieb on March 5 announced his planned resignation, the Department of Health and Human Services (HHS) said, and plans to step down in one month. Gottlieb won bipartisan support for his efforts to curb the use of flavored e-cigarettes by youths, speed approval times for cheap generic ...
FDA to Convene Meeting on CBD
On Feb. 27, FDA (U.S. Food and Drug Administration) Commissioner Scott Gottlieb, MD announced the agency’s intention to convene a public meeting in April 2019 on the development of a regulatory pathway for the use of cannabidiol (CBD) in dietary supplement and food products. The announcement came during the Commissioner’s testimony at a hearing of ...
FDA Takes Action Against Products Claiming to Treat Disease, Seeks to Strengthen Oversight
On Feb. 11, the U.S. Food and Drug Administration (FDA) posted 12 warning letters and 5 online advisory letters to foreign and domestic companies that are illegally selling more than 58 products, many that are sold as dietary supplements, which are unapproved new drugs and/or misbranded drugs that claim to prevent, treat or cure Alzheimer’s disease and a ...
NYC Orders Restaurants to Stop Serving CBD
According to CNBC, New York City’s health department has ordered restaurants to stop adding CBD to food and drinks, threatening to thwart the budding trend. Bars, cafes and restaurants across the city have been increasingly adding CBD, short for cannabidiol, to cocktails, coffee and food. New York City’s health department started cracking down on restaurants ...
Government Shutdown Impacts FDA and Industry Operations
As the government shutdown continues, FDA (Food and Drug Administration) recently announced that agency operations will continue to the extent permitted by law, maintaining core functions that address imminent threats to the safety of human life as well as activities funded by carryover user fee funds. FDA will continue to respond to emergencies—such as monitoring ...
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