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A Primer on AHPA’s Good Agricultural and Collection Practices and Good Manufacturing Practices (GACP-GMP) Guidance for Botanical Materials

What is AHPA's GACP-GMP guidance and how can it help your business?

May 22, 2018 -- 1:00-3:00 PM EST -- Member cost: $150. Nonmember cost: $350.
AHPA staff participate in panels on pesticides and food adulteration prevention at GMA Science Forum

AHPA staff participate in panels on pesticides and food adulteration prevention at GMA Science Forum

AHPA President Michael McGuffin presented on a panel discussing pesticide issues

AHPA President Michael McGuffin and Chief Science Officer Holly Johnson, Ph.D. presented at the Grocery Manufacturers Association (GMA) Science Forum held this week in Washington, DC.
AHPA comments to FWS provide recommendations for CITES

AHPA comments to FWS provide recommendations for CITES

Annotation for American ginseng should exclude sliced roots from CITES export and import controls

In comments submitted to U.S. Fish and Wildlife Service (FWS), AHPA requested that the agency propose at the 18th Conference of the Parties (CoP18) of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) to amend the annotation for American ginseng (Panax quinquefolius) to exclude sliced roots from CITES export and import controls.

AHPA participates in AOAC International Stakeholder Panel for Dietary Supplements

Four new SMPRs were approved and new calls for methods will be announced soon for kava, resveratrol, and skullcap

AHPA Chief Science Officer Holly Johnson, P.h.D, represented AHPA member interests at AOAC International's Stakeholder Panel for Dietary Supplements held in Washington, DC last week. The panel was chaired by Darryl Sullivan at AHPA member company Covance and Brian Schaneberg, director QA - regulatory, at member company Starbucks served as vice chair of the panel.

Leading North American herb associations promote Good Agricultural and Collection Practices

GACPs provide a framework to help growers, harvesters, and processors ensure quality

The American Herbal Products Association (AHPA) and the Canadian Herb, Spice and Specialty Agriculture Association (HSSA) encourage the use of recognized Good Agricultural and Collection Practices in the North American herbal products market.

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.
Day on the Hill

Day on the Hill

AHPA partners with CRN to produce this unique advocacy opportunity

AHPA member company executives—including company presidents, regulatory experts, and government relations executives—with a vested interest in legislative activity in Congress—fly in from across the nation, for a full day of networking and discussions with members of Congress and their staff. 

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.
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