Statistical Modeling for Quality Risk Assessment of Clinical Trials: Follow-Up at the Era of Remote Auditing
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Public Health, Environmental and Occupational Health,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Link
https://link.springer.com/content/pdf/10.1007/s43441-022-00388-y.pdf
Reference9 articles.
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2. Zou M, Barmaz Y, Preovolos M, et al. Using statistical modeling for enhanced and flexible pharmacovigilance audit risk assessment and planning. Ther Innov Regul Sci. 2021;55:190–6. https://doi.org/10.1007/s43441-020-00205-4.
3. Yeo IK, Johnson RA. A new family of power transformations to improve normality or symmetry. Biometrika. 2000;87(4):95. https://doi.org/10.1093/biomet/87.4.954.
4. James G, Witten D, Hastie T, Tibshirani R. An introduction to statistical learning. New York: Springer; 2013.
5. Bergmeir C, Benítez JM. On the use of cross-validation for time series predictor evaluation. Inf Sci. 2012;191:192–213. https://doi.org/10.1016/j.ins.2011.12.028.
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