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Seminars

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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.

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.

CA Prop 65 Webinar: Update on Regulatory, Compliance and Litigation Developments

An overview of several significant developments related to Prop 65

Companies that sell products in California should understand these recent changes and be prepared for additional changes that are in development. A solid compliance plan will help your company mitigate the risk of expensive litigation.

Claims substantiation webinar

Ensure supplement claims are truthful, legal, substantiated, and will help maximize your marketing

To help the supplement industry comply with the law while maximizing sales, this webinar will provide an overview of claims requirements and how to avoid the potholes of noncompliance. A panel of industry lawyers and a representative from FTC will address legal standards, today’s regulatory environment and the lawsuit risks and liabilities marketers face if claims are not adequately supported.

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.

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.

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.

NDI Notification Practical: How to Submit an NDI Notification Without Objection

How to successfully traverse the NDI notification process and avoid common pitfalls

Recorded May 9, 2017 - Member cost: $199. Nonmember cost: $399.

Webinar Recording: Claims substantiation

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

Recorded March 28, 2017 - Member cost: $199. Nonmember cost: $399.

FSMA Direct Impacts to Most AHPA Members

Regulatory experts provide a road map to FSMA understanding requirements and compliance

Webinar recorded Dec. 15, 2016. Member cost: $199. Nonmember cost: $499.

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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.




          
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