Engage, Learn, and Inspire!

The United States Pharmacopeial Convention (USP) will host a hybrid (in-person and online) Dietary Supplements & Herbal Medicines Stakeholder Forum on Wednesday, June 5, 2024, from 9:00 a.m. - 5:00 p.m. EDT. Please join USP, regulators, researchers, and industry professionals as we gather stakeholder feedback to contribute to the future of USP dietary supplement and herbal medicines standards. This year, we are also hosting a hybrid USP training session, “Taking the Guesswork out of Quality,” on June 6. Read below to learn more!

Stakeholder Forum

Onsite and online, June 5, 2024, 9 a.m. – 5 p.m. EDT

Advance registration is required; the Stakeholder Forum on June 5 is free, and lunch is included for onsite participants.

DRAFT AGENDA REGISTER NOW SPEAKER BIOS COMING SOON

Some of the topics scheduled for discussion: 

Chewable gels (gummies) issues & solutions
Botanicals: Establishing identification and specifications
Probiotic-containing dietary supplements: Unique quality challenges
Warning letters: Approaches to improving GMP compliance in specification development and testing.
USP updates and outlook

Hear from experts including:

Kate Banaszewski,NOW
Grace Bandung, Eurofins
Steven Casper, FDA
Robert Durkin, AGG
Kit Goldman, USP
Holly Johnson, AHPA
Duffy Mackay, CHPA
Maria Monagas, USP
Elan Sudberg, Alchemist

Encouraged to participate: 

Dietary supplement manufacturers
Retailers and Trade Associations
Regulators
Service providers and other interested parties who work with dietary supplements.

Full-Day HYBRID Training Session

DRAFT AGENDA REGISTER NOW

Taking the Guesswork out of Quality

Onsite and online, June 6, 2024, 9 a.m. – 5 p.m. EDT

Having trouble understanding what specifications are needed? Learn how to set the right specifications.
Wondering what changes to a method you can make before it needs to be re-validated?
Interested in case studies on developing specifications for botanicals, non-botanicals, and probiotics ingredients?

Join us for a full-day hybrid training session on USP’s quality tools for dietary supplement manufacturers and how they can make your life easier. Participants will engage with USP’s scientists to learn what’s needed in method validation and specification setting for GMP compliance. Onsite participants will also join USP staff on a tour of USP’s Rockville, MD facilities.

This training is designed for individuals in quality assurance, quality control, production, and management who already have a basic general understanding of GMP requirements.

Advance registration is required. A nominal fee of $199.00 will be charged for the USP training session, and lunch is included for onsite participants.