American Herbal Products Association (AHPA) > News > Latest News

CRN/ACI Annual Legal, Regulatory and Compliance Forum on Dietary Supplements

In-depth discussions on the myriad legal, regulatory, and compliance obligations that impact business decisions

Jun 26-28, 2017 -- New York City

Dietary Supplements Seminar

A collaborative event featuring updates and insights from FDA and Industry

May 10, 2017, 10 a.m. – 5 p.m. -- North Bethedsa, MD

Trump administration regulatory stop and review in the February 2017 AHPA Report!

February 2017 AHPA Report

AHPA expresses support for synthetic cannabinoids being placed into schedule I

AHPA submits comments to DEA

The American Herbal Products Association (AHPA) expressed strong support for the Drug Enforcement Agency (DEA) using its temporary scheduling authority to place synthetic cannabinoids into schedule I in comments submitted to the agency.

AHPA responds to inaccurate media coverage of curcumin mini-perspective

Mini-perspective has been misinterpreted to create inaccurate headlines and articles that misinform the public about turmeric

AHPA Chief Science Officer Maged Sharaf, Ph.D., responded to inaccurate media coverage of a mini-perspecive, "The Essential Medicinal Chemistry of Curcumin,"

Sharaf to discuss AHPA initiatives at 17th annual ICBS in Mississippi

Takeaways from FDA inspections webinar and DEA regulations regarding tableting, encapsulating equipment in the January 2017 AHPA Report!

January 2017 AHPA Report

IADSA update on international supplement regulations

IADSA December 2016 Newsflash

This issue of the IADSA Newsflash includes an update on the Association of Southeast Asian Nations (ASEAN) Agreement on Regulatory Framework for Health Supplements deadline for implementation, which will be pushed back to March 2023.

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.

FDA Inspections, Warning Letters and Emerging cGMP Compliance Issues

Learn the elements of 21 CFR 111 / current Good Manufacturing Practice (cGMP) regulations that FDA inspections have been focusing on recently

Webinar recorded Dec. 13, 2016. Member cost: $199. Nonmember cost: $499.

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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.