American Herbal Products Association (AHPA) > Education > Webinars

Upcoming Webinars

Webinar: How to Become Compliant with FSMA’s FSVP

The Food Safety Modernization Act’s (FSMA) rule on Foreign Supplier Verification Program (FSVP) for importers impacts most AHPA members in some way

Feb. 28, 2017 - 1:00-3:00 PM EST. Member cost: $199. Nonmember cost: $399.

Webinar: Claims substantiation

Ensuring your dietary supplement claims are truthful, substantiated and will help sell your product

March 28, 2017 - 1:00-3:00 PM EST. Member cost: $199. Nonmember cost: $399.

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Webinar Recordings

cGMP Compliance Series: Record Keeping, Document Control & How to Write SOPs

Presented: May 28, 2009

Learn how to create, manage and control documents for good GMP practices, inspectors, auditors and safety.

CGMP Compliance Series: Setting and Meeting Specifications for Contaminants in Finished Products

Presented: January 22, 2009

Under the cGMP rule, it is the responsibility of the manufacturer to identify contaminants likely or certain to be present in or on components received and to establish limits to prevent adulteration of these components.

Sustainability & Crafting Responsible "Green" Marketing

Presented: September 18, 2008

An expert panel provide practical. first-hand knowledge and answer questions about sustainability and how to walk the walk in a “greenwashed” world.

Shelf Life Statements on Dietary Supplements

Presented: May 22, 2008

The new Good Manufacturing Practice regulations for dietary supplements require that manufacturers with shelf life statements on their labels have appropriate scientific substantiation

Good Agricultural and Collection Practice

Presented: January 31, 2008

This two-hour tele-seminar provides information on getting the best quality raw materials from the field or forest, and how the grower and wildcrafter can meet buyers’ standards.

Debriefing the FDA's cGMP Implementation Seminar

Presented: October 25, 2007

This debriefing provides expertise to answer specific questions and dispel any confusion that arose from the FDA overview of cGMP implementation guidance.

Serious Adverse Event Reporting (SAER): Strategies for Compliance

Presented October 16, 2007

AHPA presents strategic regulatory, medical and legal perspectives to help companies comply with the Dietary Supplement and Nonprescription Drug Consumer Protection Act

cGMP Compliance Series: Good Manufacturing Practices: The Final Rule

Presented: July 12, 2007

This educational event will help you learn exactly what you need to know about the dietary supplement cGMP requirements, including the necessary processes and procedures need to ensure compliance.

Structure/Function Claims: Crafting Smart & Lawful Marketing Info & Labels

Presented: June 28, 2007

The limits placed on what you can and cannot claim about your product are key elements of the laws that affect dietary supplements. Every marketing plan must balance what federal law allows, what is informative to consumers, and what may drive sales.

cGMP Compliance Series: The Quality Unit

Presented: December 14, 2006

As described in the cGMP rules, your company must establish a Quality Unit, an independent group with unique responsibilities and authority to manage product excellence, consumer safety, compliance, company liability.
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2017 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.