Masterstudiengang "Drug Regulatory Affairs"
Master-Thesis
Prüfungsarbeiten
Die Zusammenfassungen der "Master-Thesis" der Studierenden des Masterstudienganges "Drug Regulatory Affairs" können hier nach einem Stichwort durchsucht werden.
Muster für das Titelblatt und die Gliederung der "Master-Thesis" so wie für das elektronische Summary finden Sie hier:
| Jahr | Name | Master-Thesis | Volltext | |
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| 2013 | Dr. Thomas Flötotto | Classification of Antiseptics and Disinfectants for Human use. The Demarcation between Biocides, Medicinal Products, Medical Devices and Cosmetics *** |
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| 2013 | Silvia Gonzalez | FDASIA "breakthrough" drug therapies – a real regulatory breakthrough for innovations? *** |
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| 2013 | Gilda Gordon | A critical review of the current marketing authorisation transfer procedure in Europe *** |
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| 2013 | Karin Hoffmann | The Etiology of BSE and Variant Creutzfeldt-Jacob Disease in Context with the new European Legislation for Material of Animal Origin, Commission Regulation (EU) No. 722/2012 Regulatory and Scientific Experience after the first BSE/vCJD Outbreak *** |
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| 2013 | Dr. Martin Hornberger | The non-clinical and clinical Implications of Drug-induced Liver Injury – Test Systems, Clinical Research and Regulatory Aspects *** |
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| 2013 | Dr. Svenja Johannsen | The Special Role of Norway and Iceland in Regulatory Affairs as EEA but not EU Members (To be or not to be "a full member" - that is the question) *** |
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