On January 30, 2018, at 04:00 pm CET, the quality assurance company Intertek is holding a webinar entitled “The impact of the EU NIAS regulations on the U.S. FDA final articles indirect food additives compliance.” The webinar addresses “key elements of the regulations” covering non-intentionally added substances (NIAS), as well as challenges in the identification and quantification of NIAS. Further, toxicological risk assessment of NIAS to evaluate “potential health risk associated with the final material or article in accordance with internationally recognized scientific principles” will be discussed. Registration is available on the event website.
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Intertek (2018). “The impact of the EU NIAS regulations on the U.S. FDA final articles indirect food additives compliance.”
