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The answer depends on individual health goals and circumstances
34 , 396407.e6 (2022)
DOI: 10.1210/jc.2011-0089 Teichman, S.L., et al
Regulatory agencies such as the FDA and EMA classify live modified microorganisms as higher-risk biological products, necessitating extensive preclinical safety evaluation, including assessment of genetic stability, exclusion of horizontal gene transfer, immunogenicity testing, and environmental biosafety analyses (Rouanet et al., 2020
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Avoid direct skin contact, inhalation, or accidental mucosal exposure during laboratory handling
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