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You walk the field, you pick some product, and you drop it off at the lab for testing. Not long after, you hear back your sample is presumptive. Now what?
This webinar discussed what changes are coming with the SQF Code Edition 9. In addition, we identified what is needed to bring your programs up to date with this new code.
In this presentation, USP and Eurofins Microbiology provided an overview of USP microbiology methods tests for microbial contamination in dietary supplements, CBD/hemp products, and probiotics. The session included an in-depth discussion regarding the importance of suitability testing, and a comparison of USP methodology to AOAC/FDA BAM methodology. USP also provided an update on new USP chapters and shared insight on what is on the horizon for USP methods.
This presentation is focused on potential hemp regulations and their related dietary supplement regulations. Some topics during this discussion include section 321(ff)(3)(B) of the FD&C Act and its impact on hemp ingredients, new dietary ingredient requirements and preparation to meet federal regulations for dietary supplements, including dietary supplement Good Manufacturing Practices, should FDA or Congress recognize hemp extracts as lawful dietary ingredients.
Partnering for Success in the China Consumer and Ingredient Markets: A New Product Pipeline to China
This online presentation announces the establishment of a groundbreaking partnership. Backed by a grant from the US Department of Commerce, the United Natural Products Alliance (UNPA) and National Animal Supplement Council (NASC) have partnered with the China Society for Inspection and Testing (CSIT) and Eurofins to establish a qualification program focused on high-quality botanical and nutritional ingredients from China, and to provide new direct access to the Chinese consumer market for US dietary supplements for humans and pets.
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