
(AGENPARL) – SILVER SPRING mar 30 maggio 2023 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
Fonte/Source: http://www.fda.gov/drugs/fdas-labeling-resources-human-prescription-drugs/patient-medication-information