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. 2024 Feb 11;17(2):235. doi: 10.3390/ph17020235
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