Development times, clinical testing, postmarket follow-up, and safety risks for the new drugs approved by the US food and drug administration: the class of 2008.
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The past 10 years of gastroenterology and hepatology-reflections and predictions.FDA designations for therapeutics and their impact on drug development and regulatory review outcomes.Association between the use of selective serotonin reuptake inhibitors and multiple sclerosis disability progression.Benefit, Risk, and Outcomes in Drug Development: A Systematic Review of Sunitinib.Comparison of the new Japanese legislation for expedited approval of regenerative medicine products with the existing systems in the USA and European Union.Characteristics and follow-up of postmarketing studies of conditionally authorized medicines in the EU.Use of the conditional marketing authorization pathway for oncology medicines in Europe.Magnitude of Clinical Benefit of Cancer Drugs Approved by the US Food and Drug Administration.Painful decision-making at FDA
P2860
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P2860
Development times, clinical testing, postmarket follow-up, and safety risks for the new drugs approved by the US food and drug administration: the class of 2008.
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article científic
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article scientifique
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articol științific
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articolo scientifico
@it
artigo científico
@gl
artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Development times, clinical te ...... nistration: the class of 2008.
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type
label
Development times, clinical te ...... nistration: the class of 2008.
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prefLabel
Development times, clinical te ...... nistration: the class of 2008.
@en
P1476
Development times, clinical te ...... nistration: the class of 2008.
@en
P2093
Curt D Furberg
Thomas J Moore
P356
10.1001/JAMAINTERNMED.2013.11813
P577
2014-01-01T00:00:00Z