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Legal Alerts >> News on dietary supplement laws, regulations and enforcement

Science Alerts >> The latest research on herbs and botanicals

Market Alerts>> Herbal market trends and AHPA-member press releases

Media Alerts >> Media coverage of the herbal industry

Medicinal Cannabis Alerts >> The latest research and news about medical cannabis

Cosmetic Alerts >> Regulatory updates and personal care product news

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IADSA update on international supplement regulations

IADSA February 2018 Newsflash

This issue of the IADSA Newsflash includes an update on France's new maximum levels for vitamins and minerals in supplements

AHPA recommends regulatory improvements in comments submitted to CFSAN

Recommendations seek to reduce regulatory burdens while maintaining consumer protections

The American Herbal Products Association (AHPA) submitted nearly 100 pages of comments today to the Food and Drug Administration (FDA) Center for Food Safety and Applied Nutrition (CFSAN) identifying numerous ways to improve regulations, guidance documents, and enforcement practices to protect public health more effectively and efficiently.

Technical issues prevent FDA from evaluating majority of recent NDI notifications

AHPA NDI Resources can help you avoid costly pitfalls

Nearly four of five new dietary ingredient (NDI) notifications recently submitted to the Food and Drug Administration (FDA) had technical issues that prevented FDA from being able to determine safety, according to AHPA's NDI Database.

Handbook promotes safe use of herbs to prevent drug interactions

Botanical Safety Handbook features extensive data on herb safety

To help ensure the safe use of herbal supplements and prevent drug interactions, the American Herbal Products Association (AHPA) produced the Botanical Safety Handbook to summarize the latest research on the safety of more than 500 species of herbs.

Organic industry leaders issue updated guidance on organic dietary supplements

Guidance on organic regulatory requirements, from farm to packaged product

The American Herbal Products Association (AHPA), the Organic Trade Association (OTA) and Quality Assurance International Inc. (QAI) announce the availability of an updated, free resource for the health supplement industry titled Guidance on Formulation and Marketing of Dietary Supplements Under the National Organic Program (NOP).

AHPA welcomes Dr. Holly Johnson as new Chief Science Officer

Dr. Johnson is a pharmacognosist with more than 20 years of experience

McGuffin statement on Sen. Hatch retirement

DSHEA was a remarkable achievement, made possible in large part by Sen. Hatch’s persistence and hard work

American Herbal Products Association (AHPA) President Michael McGuffin issued the following statement regarding the retirement of Sen. Orrin Hatch (R-UT), a vocal dietary supplement advocate who helped shape the laws that regulate the industry.

Industry Coalition Reminds Consumers, Retailers, and Product Marketers that Dietary Supplements Cannot Claim to Treat Opioid Addiction

Industry trade associations have been consistent in taking strong positions against marketing dietary supplements for treatment or prevention of diseases

The dietary supplement industry is aware of growing concerns regarding significant negative health impacts associated with opioid addiction and abuse. The leading trade associations of the dietary supplement industry support the responsible marketing and use of health-promoting vitamins, minerals, herbs, sports nutrition, and other dietary supplements.

AHPA mourns the passing of Jim Duke, a leading authority on herbal medicine

Bestselling author of The Green Pharmacy made invaluable contributions to the herbal community

AHPA was saddened to learn of the passing of James (Jim) A. Duke, Ph.D, a leading authority on herbal medicine who made invaluable contributions to the herbal products community.

AHPA submits comments on pre-DSHEA dietary ingredient list

AHPA recommended that FDA make significant changes to previous positions on new dietary ingredients (NDIs)

AHPA's comments were submitted in response to FDA's request for input on issues related to the future development of a list of dietary ingredients marketed in the United States prior to October 15, 1994, when the Dietary Supplement Health and Education Act (DSHEA) became law.

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