Works matching DE "EUROPEAN Union. European Medicines Evaluation Agency"
Results: 10
EMEA Tackles ‘Generic’ Biologic Drug Issues.
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- JNCI: Journal of the National Cancer Institute, 2006, v. 98, n. 7, p. 435, doi. 10.1093/jnci/djj145
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- Article
FDA and EMEA pool scientific advice.
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- Nature Biotechnology, 2004, v. 22, n. 12, p. 1490, doi. 10.1038/nbt1204-1490
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- Article
Decisions by regulatory agencies: are they evidence-based?
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- Trials, 2007, v. 8, p. 1, doi. 10.1186/1745-6215-8-13
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- Article
An Agency Fore-warned Is an Agency Fore-armed.
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- Applied Clinical Trials, 2004, v. 13, n. 3, p. 30
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- Article
Biosimilars; the boundaries of obviousness; and a caution on experiments conducted for litigation.
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- Journal of Generic Medicines, 2006, v. 3, n. 3, p. 233, doi. 10.1057/palgrave.jgm.4940124
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- Article
The review of drug applications submitted to the European Medicines Evaluation Agency: frequently raised objections, and outcome.
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- European Journal of Clinical Pharmacology, 2002, v. 58, n. 9, p. 573, doi. 10.1007/s00228-002-0532-8
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- Article
Biosimilars: the impact of their heterogeneity on regulatory approval.
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- Nature Reviews Drug Discovery, 2007, v. 6, n. 3, p. 1, doi. 10.1038/nrd2093-c1
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- Article
Batches of strangles vaccine withdrawn.
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- Veterinary Record: Journal of the British Veterinary Association, 2007, v. 160, n. 4, p. 104, doi. 10.1136/vr.160.4.104
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- Article
European Medicines Evaluation Agency.
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- Indian Journal of Pharmacology, 2004, v. 36, n. 1, p. 50
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- Article
First transgenic drug.
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- Chemistry & Industry, 2006, n. 12, p. 6
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- Article