Drug-Review Deadlines and Safety Problems
Author:
Publisher
Massachusetts Medical Society
Subject
General Medicine
Link
http://www.nejm.org/doi/pdf/10.1056/NEJMc086158
Cited by 14 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Internal Deadlines, Drug Approvals, and Safety Problems;American Economic Review: Insights;2021-03-01
2. Postmarket Safety Outcomes for New Molecular Entity (NME) Drugs Approved by the Food and Drug Administration Between 2002 and 2014;Clinical Pharmacology & Therapeutics;2017-12-20
3. Safety related label changes for new drugs after approval in the US through expedited regulatory pathways: retrospective cohort study;BMJ;2017-09-07
4. Assessment of the impact of scheduled postmarketing safety summary analyses on regulatory actions;Clinical Pharmacology & Therapeutics;2016-03-31
5. Assessment of Postmarketing Safety-Related Regulatory Actions in Japan;Pharmaceutical Medicine;2012-12
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