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Pharmaceutical sciences / Prescription Drug User Fee Act / Adverse Event Reporting System / ClinicalTrials.gov / Center for Biologics Evaluation and Research / Federal Food /  Drug /  and Cosmetic Act / Unique Device Identification / Validation / Direct-to-consumer advertising / Food and Drug Administration / Medicine / Health
Pharmaceutical sciences
Prescription Drug User Fee Act
Adverse Event Reporting System
ClinicalTrials.gov
Center for Biologics Evaluation and Research
Federal Food
Drug
and Cosmetic Act
Unique Device Identification
Validation
Direct-to-consumer advertising
Food and Drug Administration
Medicine
Health

FDAAA Accomplishments – One Year After Enactment

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