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In the December 18, 2014, Federal Register, FDA proposed a rule amending its prescription drug and biological product labeling regulations to require electronic distribution of the prescribing information...
United StatesFood, Drugs, Healthcare, Life Sciences
In the December 18, 2014, Federal Register,
FDA proposed a rule amending its prescription drug and biological
product labeling regulations to require electronic distribution of
the prescribing information for health care professionals, which is
currently distributed in paper form on or within the package.
Comments due March 18, 2015.
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