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FDA
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FDA is proposing to amend its human prescription drug labeling regulations to require a new type of Medication Guide—"Patient Medication Information”—for prescription drug products used, dispensed, or administered on an outpatient basis, including blood and blood components transfused in an outpatie
Baca selengkapnya di : http://www.fda.gov...
Baca selengkapnya di : http://www.fda.gov...