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doi: 10.1080/09553002.2018.1484194 74 MathiasD.MitchelR

Core safety evaluations typically encompass strain identification and characterization, pathogenicity and toxicity assessment, and contaminant screening ( Within the United States, probiotic regulation falls under the authority of the FDA, which generally classifies these products as dietary supplements or food ingredients in accordance with the Dietary Supplement Health and Education Act (DSHEA) of 1994 (566)

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from molecular stabilisation and encapsulation to biomarker modulation at the wound site, supporting its potential as an advanced platform for oxidative wound management