Events - AHPA - American Herbal Products Association (AHPA)

Technical Workshops

AHPA regularly presents in-person technical workshops to train the herbal products industry on the latest tools and methods that help ensure high-quality products and compliance with federal and state regulations.

Upcoming Events

How to Submit an NDI Notification Without Objection

Attendees receive complementary access to AHPA's NDI Database

Attend this webinar to learn how to successfully traverse the NDI notification process and avoid common pitfalls that can result in FDA objections.

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

Two-part webinar will provide insights into recent cGMP inspection trends

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

Two-part webinar will provide insights into recent cGMP inspection trends

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.
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The Cleveland Clinic's Galina Roofener to Keynote 7th Annual AHPA Botanical Congress

The Cleveland Clinic's Galina Roofener to Keynote 7th Annual AHPA Botanical Congress

Presented in cooperation with the American Botanical Council

Nov. 10, 2018 - SupplySide West - Mandalay Bay -- Las Vegas

Author: AHPA Staff
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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?

Recorded May 22, 2018 -- Member cost: $150. Nonmember cost: $350.

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AHPA Events at SupplySide West

Mandalay Bay Convention Center -- Las Vegas

Join AHPA for committee meetings, the member reception and the Botanical Congress
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AHPA meetings and events at Natural Products Expo West

AHPA Annual Member meeting, reception, awards, committee meetings and more!

March 5-8, 2018 -- Anaheim Convention Center, California

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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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The most common FDA cGMP inspection observations of 2016-17

The most common FDA cGMP inspection observations of 2016-17

Data suggests inspections and compliance continues to increase

Data from the most recent FDA inspections of dietary supplement facilities conducted in 2016 and 2017 show FDA continues to inspect an increasing number of facilities annually and the industry continues to get better at communicating compliance to FDA inspectors.
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CA Prop 65: Regulatory, Compliance and Litigation Developments

An overview of the clear and reasonable warning regulation, including recent changes and amendments

Recorded July 25, 2017 -- Member cost: $199. Nonmember cost: $399.

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2018 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.