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Regulation of Dietary Supplements

Regulation of Dietary Supplements Device "Fast Track" Plan: The FDA The has issued an advance no¬ same standard the NLEA for agency requires has a to tice of that out¬ conventional foods. The intends developed plan designed speed proposed rule-making agency review of critical medical devices lines some issues and concerns about to work with food and man¬ up supplement ufacturers and the scientific at the same that and seeks community while, time, ensuring dietary supplements public these the close comment about how the should on additional health claims that should get products scrutiny agency labels. to assure their and ef¬ to ensure their be on necessary safety regulate supplements permitted Further information is in fectiveness. The of the is to The FDA has no reason for con¬ provided goal plan safety. Federal make new medical devices cern about the of the June (58: Register promising safety moderate-po¬ 18,1993, Comments due available for use as as is rea¬ labeled vitamin and min¬ are tency, 33690). by August quickly properly the does have eral But 1993. sonably possible. products. agency 17, The new has four elements: ex¬ concerns about other market¬ plan products that contain FDA Information Available CD\x=req-\ risk assessment of new ed http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png JAMA American Medical Association

Regulation of Dietary Supplements

JAMA , Volume 270 (6) – Aug 11, 1993

Regulation of Dietary Supplements

Abstract

Device "Fast Track" Plan: The FDA The has issued an advance no¬ same standard the NLEA for agency requires has a to tice of that out¬ conventional foods. The intends developed plan designed speed proposed rule-making agency review of critical medical devices lines some issues and concerns about to work with food and man¬ up supplement ufacturers and the scientific at the same that and seeks community while, time, ensuring dietary supplements public these the close...
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Publisher
American Medical Association
Copyright
Copyright © 1993 American Medical Association. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to Government Use.
ISSN
0098-7484
eISSN
1538-3598
DOI
10.1001/jama.1993.03510060031011
Publisher site
See Article on Publisher Site

Abstract

Device "Fast Track" Plan: The FDA The has issued an advance no¬ same standard the NLEA for agency requires has a to tice of that out¬ conventional foods. The intends developed plan designed speed proposed rule-making agency review of critical medical devices lines some issues and concerns about to work with food and man¬ up supplement ufacturers and the scientific at the same that and seeks community while, time, ensuring dietary supplements public these the close comment about how the should on additional health claims that should get products scrutiny agency labels. to assure their and ef¬ to ensure their be on necessary safety regulate supplements permitted Further information is in fectiveness. The of the is to The FDA has no reason for con¬ provided goal plan safety. Federal make new medical devices cern about the of the June (58: Register promising safety moderate-po¬ 18,1993, Comments due available for use as as is rea¬ labeled vitamin and min¬ are tency, 33690). by August quickly properly the does have eral But 1993. sonably possible. products. agency 17, The new has four elements: ex¬ concerns about other market¬ plan products that contain FDA Information Available CD\x=req-\ risk assessment of new ed

Journal

JAMAAmerican Medical Association

Published: Aug 11, 1993

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