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- Hok Pang, Meng Wang, Christopher Kiff, Mira Soni, Dara Stein, and David Tyas.
- Bristol-Myers Squibb Pharmaceuticals Ltd., London, UK.
- Drug Discov. Today. 2019 Dec 1; 24 (12): 2231-2233.
AbstractReal-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.Copyright © 2019 Elsevier Ltd. All rights reserved.
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