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Webinars

 

Upcoming Webinars:

  • Artificial Intelligence (AI) in Animal Health & Nutrition with Eurofins Testing Solutions
    Agriculture 5.0 - PART 2

    • Thursday, July 18, 2024 @ 11:00 AM CDT
    • Presenter: Leo Schilling | Sr. Scientific Services Manager Eurofins Animal Health Testing
    • Register HERE!
  • Regulation in Plain Text: FDA and USDA Regulatory Updates and What They Mean to You

    • Wednesday, August 7, 2024 @ 11:00 AM CDT
    • Presenters: Douglas Marshall | Chief Scientific Officer - Eurofins Microbiology Laboratories 
      John Scanga | Chief Scientific Officer - Eurofins North American Meat Division
    • Registration coming soon!

 

 

On-Demand Webinars:



In this informative conversation between Vanessa Snyder and Grace Bandong they discuss contaminant testing in hemp and CBD products and why it is important. Grace tells companies the importance of testing for contaminants and gives advice for when and what to test.


Eurofins presents a validation of USP <467> residual solvent methodology for testing on CBD and hemp-based products at the North American Chemical Residue Workshop.


Eurofins presents at AOAC Annual Meeting and Exposition in 2020 summarizing the modifications made to the AOAC Official Method 2018.11 for quantification of cannabinoids to include conversion of Δ9-THCA into Δ9-THC.


Eurofins develops and validates a versatile HPLC-UV/DAD method for analyzing twelve major cannabinoids in dried plant materials, concentrates and oils. Method was granted AOAC First Action OMA status (AOAC Official Method 2018.11).


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.


Your CBD and hemp-derived multiple-use cosmetic and personal care products that contain preservatives need to be tested to assure the preservation, or antimicrobial action is adequate to fight the introduction of microorganisms.


Read this article to learn more about hemp contaminant testing and how you can be prepared to correctly test your hemp-derived products.


In this article, we will make the case for a testing program for your hemp business that you can implement today that will help prepare you for the regulations to come.


Choosing a reputable hemp testing lab can be difficult and time-consuming. We have put together a checklist of information your hemp company should consider when vetting and selecting a hemp testing partner.


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