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Regulatory Oversight and Safety of Probiotic Use
Depending on intended use of a probiotic (drug vs. dietary supplement), regulatory requirements differ greatly. For dietary supplements, premarketing demonstration of safety and efficacy and approval by the Food and Drug Administration are not required; only premarket notification is required. Sacch...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Centers for Disease Control and Prevention
2010
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3294522/ https://ncbi.nlm.nih.gov/pubmed/21029521 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3201/eid1611.100574 |
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