The FDA Amendments Act of 2007 — Assessing Its Effects a Decade Later

Prescription-drug policy in the United States has developed through a process of punctuated evolution, often driven by crises. Progressive-era concern about "patent medicines" that contained primarily alcohol or opium led to mandatory labeling under the 1906 Pure Food and Drug Act. The deaths of…

Read the full post at The New England Journal of Medicine: Search Results in Health Policy and Reform
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