| 2D/3D | Two-/Three-Dimensional Cell Culture |
| 3Rs | Replacement, Reduction, and Refinement |
| ADME | Absorption, Distribution, Metabolism, and Excretion |
| AI | Artificial Intelligence |
| CFU | Colony-Forming Unit |
| DA | Defined Approach |
| DDI | Drug–drug interaction |
| DILI | Drug-Induced Liver Injury |
| EMA | European Medicines Agency |
| FDA | Food and Drug Administration |
| HCI | High-Content Imaging |
| hESC | Human Embryonic Stem Cell |
| hiPSC/iPSC | (Human) Induced Pluripotent Stem Cell |
| hiPSC-CM | hiPSC-Derived Cardiomyocyte |
| HSC | Hematopoietic Stem Cell |
| qHTS | Quantitative High-Throughput Screening |
| IATA | Integrated Approaches to Testing and Assessment |
| ISSCR | International Society for Stem Cell Research |
| LDH | Lactate Dehydrogenase |
| ML | Machine Learning |
| MPS | Microphysiological System |
| MTT | 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide |
| NAMs | New Approach Methodologies |
| NIH | National Institutes of Health |
| NRU | Neutral Red Uptake |
| OECD | Organisation for Economic Co-operation and Development |
| PBPK | Physiologically Based Pharmacokinetic (Modelling) |
| PFAS | Polyfluoroalkyl Substances |
| PI | Propidium Iodide |
| PSC | Pluripotent Stem Cell |
| QIVIVE | Quantitative In Vitro–In Vivo Extrapolation |
| QSAR | Quantitative Structure–Activity Relationship |
| ROS | Reactive Oxygen Species |
| RTCA | Real-Time Cell Analysis |
| SRB | Sulforhodamine B |
| STS | Sequential Testing Strategy |
| tcpl | ToxCast Pipeline for Curve Fitting |
| Tox21/ToxCast | U.S. Toxicology Data Programs for High-Throughput Screening |