American Herbal Products Association (AHPA) > Education > Webinars

Upcoming Webinars

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

Nov. 30 (FDA Inspections and Emerging cGMP Compliance Issues) -- Dec. 14 (Q&A and Responding to an FDA 483)

This two-part webinar will provide 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 will also provide strategies to respond to an FDA  483 in order to avoid a warning letter.

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Webinar Recordings

cGMP Compliance Series Teleseminar: Variances

Presented: November 1, 2011

Variances--an exception or departure from approved protocol--occur and this webinar will help you prepare for them.

FDA's NDI Guidance: What You Need to Know

Presented: July 19, 2011

A panel of experts help attendees understand the key elements of FDA's New Dietary Ingedient (NDI) draft guidance and how it will impact businesses in the supplement industry.

Living with Proposition 65: Preventative Measures & Defending Against a 60-Day Notice

Presented: October 18, 2010

As much as 30% of the national sales of dietary supplements may be to California consumers - but companies that market in that state may encounter high penalties for non-compliance with a California law known as Proposition 65. The focus of this law for the supplement class has been on the warnings required for products that may inadvertently contain small amounts of heavy metals, such as arsenic, cadmium, and mercury, and especially lead.

Guidance for Addressing FDA cGMP Inspections of Dietary Supplement Facilities

Understand your rights and obligations when FDA conducts a cGMP inspection

This Guidance for Addressing FDA Inspections of Dietary Supplement Facilities has been prepared to assist AHPA members in understanding their rights and obligations when the U.S. Food and Drug Administration conducts an inspection of a facility in which dietary supplements or ingredients are manufactured, processed, packed or held. It provides descriptions and analyses of the current federal laws that are relevant to inspection of dietary supplement facilities and suggestions of how to prepare for and conduct inspections in a manner that fully complies with these laws.

cGMP Compliance Series: How to Conduct & Manage a FDA Inspection

Presented: July 30, 2009

This webinar covers the extent of FDA's authority during an inspection, so you know your rights.

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

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.
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