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Eighth Annual NIE New Ingredient Awards Call for Entries

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AHPA to Host Inaugural Hemp-CBD Dietary Supplement Congress

by Shari Barbanel | July 1, 2019

The American Herbal Products Association (AHPA) is presenting a two-day Hemp-CBD Supplement Congress in Denver, CO this August to provide critical input for companies navigating the rapidly evolving legal, regulatory and financial landscapes to manufacture and market dietary supplement products with hemp or hemp-derived ingredients including cannabidiol (CBD). The event features presentations from federal officials, ...

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 ...

FDA Announces New Attention to Dietary Supplement Regulations

by Shari Barbanel | February 13, 2019

FDA (U.S. Food and Drug Administration) Commissioner Scott Gottlieb, MD, has announced that the agency is planning “new efforts to strengthen regulation of dietary supplements by modernizing and reforming FDA’s oversight,” with a goal of implementing “one of the most significant modernizations of dietary supplement regulation and oversight in more than 25 years.” The commissioner’s ...

AHPA Issues Updated Slack-fill Guidance

by Shari Barbanel | January 8, 2019

The American Herbal Products Association (AHPA) has updated its Slack-Fill Guidance to help the regulated supplement industry inform consumers and comply with all relevant federal requirements. This guidance was originally published in November 2016 and has been reorganized and edited for clarity, with one substantive revision in the discussion on “Label statements and fill lines” ...

Nutritional Supplements Access Preserved in Arizona

by Shari Barbanel | January 3, 2019

A proposal that would have drastically limited access to safe, legal and popular products for Arizonans was changed recently with the help of the Natural Products Association (NPA) and the American Herbal Products Association (AHPA), who worked with the Arizona Board of Pharmacy and other state policymakers on the issue. The proposal under consideration would have ...

Trade Associations Warn Consumers of Dangerous Substance Illegally Marketed as a Dietary Supplement

by Shari Barbanel | November 5, 2018

The dietary supplement industry sounded the alarm about the dangers of “phenibut,” a substance being illegally marketed in products fraudulently labeled as dietary supplements. Developed and used as a drug in the former Soviet Union for its supposed brain-enhancing properties, phenibut is not approved as a drug in the United States, nor does it meet ...

AHPA Launches Sustainability Subcommittee

by Shari Barbanel | October 22, 2018

The American Herbal Products Association (AHPA) Botanical Raw Materials Committee has launched a Sustainability Subcommittee to further AHPA’s ongoing efforts to ensure sustainable supplies of valuable botanicals. The subcommittee will be a vehicle for increasing awareness of sustainability issues and best practices, provide a forum to discuss and develop industry-wide standards, and promote existing sustainability ...

Excess Rain Limits Supply and Drives Up Saw Palmetto Prices

by Shari Barbanel | October 4, 2018

The American Herbal Products Association (AHPA) has been in communication with several of its members and other companies actively involved in the saw palmetto berry harvest in Florida, who contributed to this report. The harvest season began in early August in Florida and the total berry harvest for the season should be known early this ...

AHPA NDI Database Shows Increase of Recent Notifications Filed Successfully

by Shari Barbanel | August 27, 2018

Eight of the 21 new dietary ingredient (NDI) notifications released by the U.S. Food and Drug Administration (FDA) between January 1, 2018 and May 31, 2018 were filed by the agency without substantive comment. The vast majority of these (17) complied with all submission regulations (21 CFR 190.6). The recently received data have been analyzed and ...

Industry Applauds FDA Action on Highly Concentrated Caffeine

by Shari Barbanel | April 16, 2018

The U.S. Food and Drug Administration (FDA) recently took an important step to better protect consumers from the dangers of highly concentrated and pure caffeine products. These products present a significant public health threat because of the high risk that they will be erroneously used at excessive, potentially dangerous doses. Highly concentrated and pure caffeine, ...

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