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Cell Metab (2016) 24(3):44761
In Europe, the European Medicines Agency supports two main regulatory tracks: well-established use and traditional use registration under Directive 2004/24/EC, which requires data on safety, efficacy, and pharmacovigilance
Recently, an interest in this element in many biotechnology fields has increased
Human gut epithelium features recapitulated in MINERVA 2.0 millifluidic organ-on-a-chip device
[DOI] [PMC free article] [PubMed] [Google Scholar] 125.Settivari R., VanDuyn N., LeVora J., Nass R
