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Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge
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Bossi, F., et al
The GLP-1 era is therefore accelerating portfolio discipline decisions that many companies were already overdue to make, which means the question is not really whether to rationalize but whether to do it on the companys own terms or under duress
doi: 10.1016/j.bcp.2023.115830 61 Galicia-MorenoMMonroy-RamirezHCCaloca-CamarenaFArceo-OrozcoSMurielPSandoval-RodriguezAet al
4 More recently, the FDA Reauthorization Act of 2017 (FDARA) made a reference encouraging the enrollment of more diverse patient populations, and the Final Rule for Clinical Trials Registration and Results Information Submission (42 CFR Part 11) went into effect in January 2017
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