Correction: Regulatory Considerations Toward Orphan Drug Designation and Orphan Drug Exclusivity in the United States and European Union: Structural Similarity, Clinical Superiority/Significant Benefit, and Case Studies
Ther Innov Regul Sci
.
2023 Mar;57(2):396-398.
doi: 10.1007/s43441-022-00487-w.
Authors
Scott W Roberts
1
,
Tara Laura Brandt Elvang
2
,
Laila Syed
2
,
Marianne Bork Samuelsen
2
,
Eva Lisby Arp-Hansen
2
,
Henrik Kim Nielsen
2
,
Ida Katrine Lund
2
,
Dorte Lunøe Dünweber
2
,
Nicolai Listov-Saabye
2
,
Dorte Bjørn-Larsen
2
,
Anette Hjelmsmark
2
,
Tue Anker Mikkelsen
2
Affiliations
1
Regulatory Affairs, Novo Nordisk A/S, Vandtårnsvej 114, 2860, Søborg, Denmark.
[email protected]
.
2
Regulatory Affairs, Novo Nordisk A/S, Vandtårnsvej 114, 2860, Søborg, Denmark.
PMID:
36472778
DOI:
10.1007/s43441-022-00487-w
No abstract available
Publication types
Published Erratum