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AHPA issues Status Report and schedules webinar on hemp and CBD after Farm Bill passage

Farm bill includes provisions to legalize hemp

Congress passed yesterday a Farm Bill that includes historic provisions that will legalize hemp, the low THC cultivars of the Cannabis sativa L. species. This landmark legislation will change how hemp and hemp-derived products like cannabidiol (CBD) are regulated in the U.S. To help the herbal products industry understand the new regulatory landscape, AHPA has produced a Status Report and has scheduled a webinars to answer industry questions.

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.

CA Prop 65 Update on Regulatory, Compliance and Litigation Developments

An overview of several significant developments related to Prop 65

Recorded September 20, 2018 -- Duration: 2 hours

Claims substantiation webinar

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

Recorded Aug. 21, 2018 -- Member cost: $199. Nonmember cost: $399.

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.

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.

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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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