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Recent regulatory guidance documents, such as the 2025 Australian Therapeutic Goods Administration (TGA) guidance on the quality of listed probiotic medicines and broader discussions on LBPs from 2020, underscore the necessity for strain-level identification, validated enumeration techniques, and explicit labeling of potency and storage conditions (570, 571)

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Higher pricing does not automatically indicate better quality, but it often correlates with clearer testing disclosure, stronger documentation, and more consistent batch-level verification