Document Type
Article
Publication Date
10-18-2013
Keywords
Human Microbiome Project, HMP, biologics, regulation
Abstract
Some products marketed as drugs should be excused from Phase I trials, but safety and efficacy claims for dietary supplements should be more tightly regulated.
Publication Citation
342 Science 6156 (2013)
Disciplines
Food Biotechnology | Food Microbiology | Medical Biotechnology | Medical Microbiology
Digital Commons Citation
342 Science 6156 (2013).
Included in
Food Biotechnology Commons, Food Microbiology Commons, Medical Biotechnology Commons, Medical Microbiology Commons
Comments
This is the authors' version of the work. It is posted here by permission of the AAAS for personal use, not for redistribution. The definitive version was published in Science Policy Forum, vol. 342, October 18, 2013. see: http://www.sciencemag.org/content/342/6156/314.full?ijkey=QUF.p5J3snuso&keytype=ref&siteid=sci
DOI: 10.1126/science.1244656