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Recent News

USDA’s final rule for GMO labeling ignores recommendations of consumers and AHPA

Final rule hinders consumer access to information on genetically modified foods

The U.S. Department of Agriculture (USDA) Agricultural Marketing Service (AMS) issued a final rule on December 20 that establishes the new national mandatory bioengineered (BE) food disclosure standard. The final rule does not incorporate significant revisions recommended by AHPA and consumer groups that were aimed at ensuring U.S. consumers can discern if their food includes genetically modified organisms (GMOs) or ingredients derived from GMOs.

Slack-Fill Guidance (Revised 2019)

This guidance helps companies inform consumers and comply with federal regulations

The American Herbal Products Association (AHPA) published slack-fill guidance in 2016 and revised the document in 2019 to help the regulated supplement industry inform consumers and comply with all relevant federal requirements.

FDA Inspection Trends, cGMP Compliance Issues and Responding to an FDA 483

Two-part webinar recorded Dec. 4 and 18

Two-part webinar will provide data on recent FDA inspections, an overview of emerging compliance issues and strategies for responding to an FDA 483 in order to avoid an FDA warning letter.

Nutritional supplements access preserved in Arizona

AHPA and NPA protect proper rules for safe, legal, natural products

A proposal that would have drastically limited access to safe, legal and popular products for Arizonans was changed recently thanks to 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.

AHPA President presents at SOHO Expo World of Hemp Forum

McGuffin provides overview of federal legal issues for hemp and hemp-derived products

AHPA President Michael McGuffin on Friday provided an overview of federal legal issues for hemp and hemp-derived products at the World of Hemp Forum held at the annual SOHO Expo in Orlando, FL.
Lessons in herb safety from The Cleveland Clinic Chinese Herbal Medicine Program

Lessons in herb safety from The Cleveland Clinic Chinese Herbal Medicine Program

Clinic reports only six mild adverse events since 2014

Nationally board-certified acupuncturist and Chinese herbalist at the Cleveland Clinic Galina Roofener shared safety data and lessons learned from the Cleveland Clinic Wellness Institute’s Traditional Chinese Herbal Medicine (TCHM) Program at her keynote delivered at the American Herbal Products Association’s (AHPA’s) 7th Annual Botanical Congress presented on Nov. 10 in Las Vegas at the SupplySide West trade show.
FDA Update by ODSP Director Steven Tave Presented at 7th Annual AHPA Botanical Congress

FDA Update by ODSP Director Steven Tave Presented at 7th Annual AHPA Botanical Congress

Tave outlines collaborations between FDA and supplement industry to ensure consumer safety

The American Herbal Products Association’s (AHPA’s) 7th Annual Botanical Congress featured a Food and Drug Administration (FDA) update by Steven Tave, FDA’s Director of the Office of Dietary Supplement Programs (ODSP), who highlighted recent collaborations between the responsible supplement industry and FDA toward the shared goal of a well-regulated dietary supplement market.
AHPA Chief Science Officer presents at Hemp Industries Association 25th Annual Conference

AHPA Chief Science Officer presents at Hemp Industries Association 25th Annual Conference

Dr. Johnson discusses quality standards for farmers, formulators, and finished product manufacturers

AHPA Chief Science Officer Dr. Holly Johnson discussed quality standards for hemp farmers, formulators, and finished product manufacturers at the Hemp Industries Association (HIA) 25th Annual Conference held Nov. 2-5 in Los Angeles.

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

Supplement industry sounds 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 the regulatory requirements to be sold in, or as, a dietary supplement. The ingredient should be considered dangerous, and has been associated with potentially serious side effects and great risk for addiction.
AHPA provides cGMP resources to herbalists attending AHG Symposium

AHPA provides cGMP resources to herbalists attending AHG Symposium

AHG awards Dr. Zimmermann for cGMP compliance poster

AHPA Chief Information Analyst Merle Zimmermann, Ph.D. provided cGMP compliance resources to herbalists attending the American Herbalist Guild (AHG) 29th Annual Symposium in Georgia last week.
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2019 Annual Fund Sponsors

  

AHPA appreciates the support of its sponsors, but does not endorse, recommend, or provide a warranty for any sponsor company, its products or services. AHPA has no responsibility for any transaction entered into with any of these companies.