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AHPA expands online Botanical Safety Handbook with new information and research

AHPA expands online Botanical Safety Handbook with new information and research

Online BSH features extensive safety information on more than 500 botanicals

AHPA has expanded several entries in the online Botanical Safety Handbook to include the latest herb safety information and research.

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

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.
Guidance on organic dietary supplements

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

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

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 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.

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

Recorded Nov. 30 and Dec. 14

This two-part webinar provides an update on the elements of current Good Manufacturing Practice (cGMP) regulations (21 CFR 111) that have been the primary focus of recent FDA inspections. Experts also provide strategies to respond to an FDA  483 in order to avoid a warning letter.

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