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. 2020 Jun 17;12(6):562. doi: 10.3390/pharmaceutics12060562
PAT Process Analytic Technology
FDA U.S. Food and Drug Administration
ICH International Conference on Harmonization
QbD Quality by Design
QbC Quality by Control
DoE Design of Experiments
iDoE intensified Design of Experiments
DoDE Design of Dynamic Experiments
QTPP Quality Target Product Profile
CQA Critical Quality Attributes
CPP Critical Process Parameters
CMA Critical Material Attributes
ANOVA Analysis of Variance
MPC Model Predictive Control
ODEs Ordinary Differential Equations
SA Sensitivity Analysis
PCA Principal Component Analysis
PLS Partial Least Square