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

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.

cGMP Compliance: Botanical Identity & Herb Quality

Presented: September 28, 2006

This webinar is designed to help companies evaluate ingredient identity and quality and comply with FDA’s dietary supplement cGMP rule.

Allowable Claims and Claim Substantiation: How to Comply with the Law & Maximize your marketing

Presented: August 3, 2006

Many companies have learned the hard way that the Federal Trade Commission (FTC) does not send Warning Letters. If your claims are out of compliance, FTC is going to file a complaint.

Claims Substantiation: How to Ensure Your Dietary Supplement Product Claims are Truthful & Lega

Presented: March 3, 2006

The FDA and FTC have stepped up their enforcement activities against unlawful drug claims and unsubstantiated structure/function claims made by supplement marketers.

Federal Food Allergen Labeling & Consumer Protection Act Seminar

Presented: December 2, 2005

Targeted and instructional information to help you efficiently learn the relevant components of the law, become trained to set up a compliance program, and hear what is at stake if products do not meet the new policy.
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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.