Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

2 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
FDA regulation of dietary supplements and requirements regarding adverse event reporting.
Frankos VH, Street DA, O'Neill RK. Frankos VH, et al. Among authors: o neill rk. Clin Pharmacol Ther. 2010 Feb;87(2):239-44. doi: 10.1038/clpt.2009.263. Epub 2009 Dec 23. Clin Pharmacol Ther. 2010. PMID: 20032973
Use of data mining at the Food and Drug Administration.
Duggirala HJ, Tonning JM, Smith E, Bright RA, Baker JD, Ball R, Bell C, Bright-Ponte SJ, Botsis T, Bouri K, Boyer M, Burkhart K, Condrey GS, Chen JJ, Chirtel S, Filice RW, Francis H, Jiang H, Levine J, Martin D, Oladipo T, O'Neill R, Palmer LA, Paredes A, Rochester G, Sholtes D, Szarfman A, Wong HL, Xu Z, Kass-Hout T. Duggirala HJ, et al. J Am Med Inform Assoc. 2016 Mar;23(2):428-34. doi: 10.1093/jamia/ocv063. Epub 2015 Jul 23. J Am Med Inform Assoc. 2016. PMID: 26209436 Review.
Feedback