Petitioning the FDA to Improve Pharmaceutical, Device and Public Health Safety by Ordinary Citizens: A Descriptive Analysis.
The United States Constitution protects the right of citizens to petition the government for "a redress of grievances." This right has important implications for citizens desiring to advance the public health by petitioning administrative agencies, such as the Food and Drug Administration,...
Main Authors: | Brian K Chen, Y Tony Yang, Xi Cheng, John Bian, Charles L Bennett |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2016-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC4865109?pdf=render |
Similar Items
-
A Comprehensive Map of FDA-Approved Pharmaceutical Products
by: Hao Zhong, et al.
Published: (2018-12-01) -
Implementation of the new FDA quality by design guidance in pharmaceutical production
by: Tozer, Stephanie Michelle
Published: (2009) -
Drugs, Devices, and the FDA: Part 1
by: Gail A. Van Norman, MD
Published: (2016-04-01) -
Gifts, Drugs, and the FDA: Cross-Disciplinary Perspectives on Physician-Pharmaceutical Interactions
by: Kayleen Papin, et al.
Published: (2009-09-01) -
The FDA guidance for industry on PROs: the point of view of a pharmaceutical company
by: Bamfi Francesco, et al.
Published: (2006-10-01)