医学
食品药品监督管理局
药品
动作(物理)
药品管理局
药理学
药物标签
重症监护医学
梅德林
药品审批
遗产管理(遗嘱认证法)
制药工业
麻醉
药物作用
受控物质
作者
Harry Doernberg,Joshua D. Wallach,Molly M. Jeffery,Maryam Mooghali,Reshma Ramachandran,Joseph S. Ross
标识
DOI:10.1001/jamainternmed.2025.6566
摘要
This cross-sectional analysis found that the enhanced safety-related regulatory authorities of FDAAA were not associated with differences in time to first postmarket safety-related action. However, among therapeutics with postmarket safety-related actions within 5 years of approval, median time to first action was shorter post-FDAAA implementation.
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