From complexity to approval in the European Union: Regulatory pathways and data challenges in the evaluation of non-oncology orphan medicines.
- DOI
- 10.1016/j.drudis.2026.104715
- Published
- 2026 Jul
- Container
- Drug discovery today
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.drudis.2026.104715,
title = {From complexity to approval in the European Union: Regulatory pathways and data challenges in the evaluation of non-oncology orphan medicines.},
author = {Andriantafika G and Janssen H and Balkowiec-Iskra E and Gartner C and Sepodes B and Van der Schueren B},
year = {2026},
journal = {Drug discovery today},
doi = {10.1016/j.drudis.2026.104715},
url = {https://doi.org/10.1016/j.drudis.2026.104715}
}RIS
TY - JOUR TI - From complexity to approval in the European Union: Regulatory pathways and data challenges in the evaluation of non-oncology orphan medicines. AU - Andriantafika G AU - Janssen H AU - Balkowiec-Iskra E AU - Gartner C AU - Sepodes B AU - Van der Schueren B PY - 2026 JO - Drug discovery today DO - 10.1016/j.drudis.2026.104715 UR - https://doi.org/10.1016/j.drudis.2026.104715 ER -
APA
G, A., H, J., E, B., C, G., B, S., & B, V. D. S. (2026). From complexity to approval in the European Union: Regulatory pathways and data challenges in the evaluation of non-oncology orphan medicines.. Drug discovery today. https://doi.org/10.1016/j.drudis.2026.104715
Source records
- pubmed · retrieved 2026-09-25T10:10:31.007Z