Early Access to Medicines Scheme: real-world data collection

被引:3
|
作者
Pang, Hok [1 ]
Wang, Meng [1 ]
Kiff, Christopher [1 ]
Soni, Mira [2 ]
Stein, Dara [2 ]
Tyas, David [1 ]
机构
[1] Bristol Myers Squibb Pharmaceut Ltd, London, England
[2] Evidera, London, England
关键词
D O I
10.1016/j.drudis.2019.06.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Real-world data (RWD) generated during the pre-approval phase could be supplementary to primary clinical trial outcomes; however, as we discuss here, a data collection framework is needed to ensure the validity and applicability of these data.
引用
收藏
页码:2231 / 2233
页数:3
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