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  • Search: subject:"Orphan designation"
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Year of publication
Subject
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Accelerated approval 3 Breakthrough therapy 3 Clinical trial 3 Drug development 3 Drug price 3 Efficacy 3 European medicines agency 3 Fast track 3 Healthcare policy 3 Innovation 3 Orphan designation 3 Pharmaceutical policy 3 Priority review 3 Safety 3 Special designation 3 US food and drug administration 3 Arzneimittel 1 Arzneimittelmarkt 1 Arzneimittelrecht 1 EU countries 1 EU-Staaten 1 Gesundheitspolitik 1 Gesundheitswesen 1 Health care system 1 Health policy 1 Medical treatment 1 Medizinische Behandlung 1 New product development 1 Pharmaceutical industry 1 Pharmaceutical law 1 Pharmaceutical market 1 Pharmaceuticals 1 Pharmacology 1 Pharmaindustrie 1 Pharmakologie 1 Produktentwicklung 1 USA 1 United States 1
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Online availability
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Free 3
Type of publication
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Article 3
Type of publication (narrower categories)
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Article 2 Article in journal 1 Aufsatz in Zeitschrift 1
Language
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English 3
Author
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Albers, Sebastian 3 Boch, Tobias 3 Michaeli, Daniel Tobias 2 Michaeli, Julia Caroline 2 Michaeli, Thomas 2 Michaeli, Christoph T. 1 Michaeli, Daniel 1 Michaeli, Julia 1
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Published in...
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The European Journal of Health Economics 2 The European journal of health economics 1
Source
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EconStor 2 ECONIS (ZBW) 1
Showing 1 - 3 of 3
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Special FDA designations for drug development : orphan, fast track, accelerated approval, priority review, and breakthrough therapy
Michaeli, Daniel; Michaeli, Christoph T.; Albers, Sebastian - In: The European journal of health economics 25 (2024) 6, pp. 979-997
Over the past decades, US Congress enabled the US Food and Drug Administration (FDA) to facilitate and expedite drug development for serious conditions filling unmet medical needs with five special designations and review pathways: orphan, fast track, accelerated approval, priority review, and...
Persistent link: https://www.econbiz.de/10015131485
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Cover Image
Special FDA designations for drug development: orphan, fast track, accelerated approval, priority review, and breakthrough therapy
Michaeli, Daniel Tobias; Michaeli, Thomas; Albers, Sebastian - In: The European Journal of Health Economics 25 (2023) 6, pp. 979-997
Background: Over the past decades, US Congress enabled the US Food and Drug Administration (FDA) to facilitate and expedite drug development for serious conditions filling unmet medical needs with five special designations and review pathways: orphan, fast track, accelerated approval, priority...
Persistent link: https://www.econbiz.de/10015328830
Saved in:
Cover Image
Special FDA designations for drug development: orphan, fast track, accelerated approval, priority review, and breakthrough therapy
Michaeli, Daniel Tobias; Michaeli, Thomas; Albers, Sebastian - In: The European Journal of Health Economics 25 (2023) 6, pp. 979-997
Background: Over the past decades, US Congress enabled the US Food and Drug Administration (FDA) to facilitate and expedite drug development for serious conditions filling unmet medical needs with five special designations and review pathways: orphan, fast track, accelerated approval, priority...
Persistent link: https://www.econbiz.de/10015404267
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