Orphan medicinal products in Europe and United States to cover needs of patients with rare diseases: an increased common effort is to be foreseen
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Genetics (clinical),General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s13023-017-0617-1.pdf
Reference37 articles.
1. European Parliament and of the Council Regulation (EC) 141/2000 of 16 December 1999 on Orphan Medicinal Products. OJL 018/1, 22.01.2000.
2. Orphan Drugs Act of 1983. Public law 97-414. 97th Congress. Jan.4, 1983.
3. Seoane-Vazquez E, Rodriguez-Monguio R, Szeinbach SL, Visari J. Incentives for orphan drug research and development in the United States. Orphanet J Rare Dis. 2008;3:33.
4. Tambuyzer E. Rare diseases, orphan drugs and their regulation: questions and misconceptions. Nat Rev Drug Discov. 2010;9:921–9.
5. Hudson I, Breckenridge A. The challenges of orphan drugs and orphan diseases: real and imagined. Clin Pharmacol Ther. 2012;92(2):151–3.
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