Masterstudiengang "Drug Regulatory Affairs"
Master-Thesis
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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 | Clelia Bonadei | Obligations of economic operators, traceability, vigilance and market surveillance of medical devices as foreseen by the EU Commission Proposal for a Regulation on Medical Devices of 26 Sept. 2012: comparison with existing requirements and evaluation *** |
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| 2013 | Dr. Sarah Burrack | Status, challenges and regulatory strategies to develop a malaria vaccine *** |
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| 2013 | Claudia Callies-Klüpfel | The new European Health Claims Regulation establishing a List of permitted Health Claims: Questions around its Application and the current State of Discussion to the “Claims on Hold” and to the “Botanicals” as well as a comparative | |
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| 2013 | Esther Cónsul Tejero | Melde- und Bobachtungssystem für Medizinprodukte - eine statistische Auswertung anhand eines Beispiels | |
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| 2013 | Alex Dranov | European View on Current Regulatory Legislation in the CIS Countries. Marketing Authorisation of Herbal Medicinal Products in Russia and the Ukraine *** |
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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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