在2012年至2021年期间,对欧盟中央授权药品的额外风险最小化措施的有效性评估的持续时间

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Published on: August 30, 2018

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Sharon C M Essink1,2, Inge M Zomerdijk2, Sabine M J M Straus2,3

  • 1Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands.

Drug safety
|September 1, 2023
PubMed
概括

对欧盟药物的额外风险最小化措施 (aRMMs) 完成有效性评估比预期的要长,只有20.7%的药物在60个月内完成. 大多数研究都面临延误,影响药物安全性的及时评估.

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