| AEs | Adverse Events |
| ADAs | Anti-Drug Antibodies |
| BD | Biodisponibility |
| CHMP | Committee for Medicinal Products for Human Use |
| CQAs | Critical Quality Attributes |
| EMA | European Medicine Administration |
| EEE | European Economic Area |
| EU | European Union |
| Fab | Fragment Antigen-Binding |
| Fc | Fragment Crystallizable |
| FcRn | Neonatal Fragment Crystallizable Receptor |
| FcγR | Fragment Crystallizable-Gamma Receptor |
| FDA | Food and Drug Administration |
| FIMEA | Finnish Medicines Agency |
| GCSF | Granulocyte Colony-Stimulating Factor |
| GH | Growth Hormone |
| ICH | International Conference of Harmonization |
| INFα | Interferon Alpha |
| INFβ | Interferon Beta |
| INN | International Naming System |
| RP | Reference Product |
| WHO | World Health Organization |
| mAb | Monoclonal Antibody |
| MA | Marketing Authorization |
| MS | Member State |
| PK | Pharmacokinetic |
| PD | Pharmacodynamics |
| PTMs | Post-Translational Modifications |
| PV | Pharmacovigilance |
| QbD | Quality-by-Design |
| QTPP | Quality Target Product Profile |
| SmPC | Summary of Product Characteristics |
| tRNA | Transfer RNA |