ATMP	Advanced Therapy Medicinal Products
CBER	Center for Biologics Evaluation and Research
CDER	Center for Drug Evaluation and Research
ISEV	International Society for Extracellular
FDA	Food and Drug Administration
GMP	Good Manufacturing Practices
MSC	Mesenchymal Stem Cell
PMD	Pharmaceuticals and Medical Devices
ASRM	Act on the Safety of Regenerative Medicine
EMA	European Medicines Agency
PMDA	Pharmaceuticals and Medical Devices Agency
MFDS	Ministry of Food and Drug Safety
TFDA	Taiwan Food and Drug Administration
CDSCO	Central Drugs Standard Control Organization
ICMR	Indian Council of Medical Research
TGA	Therapeutic Goods Administration
NMPA	National Medical Products Administration
MHRA	Medicines and Healthcare Products Regulatory Agency
PHS	Public Health Service
IND	Investigational New Drug
BLA	Biologics License Application
CMC	Chemical, Manufacturing, and Control
CAT	Committee for Advanced Therapies
RMA	Regenerative Medicine Act
GTP	Good Tissue Practice
GCP	Good Clinical Practice
MISEV	Minimal Information for Studies of Extracellular Vesicles
EV	Extracellular Vesicles
MOA	Mechanism of Action
ICH	International Conference on Harmonization
CTN	Clinical Trial Notification
CTX	Clinical Trial Exemption
CTA	Clinical Trial Application
ICTRP	International Clinical Trials Registry Platform