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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| 2023 | Yvonne Hinterstocker | Comparison of the regulatory requirements for the proof of comparability of generic locally applied locally acting products with their originator product in the EU and USA - an overview on the current status and the latest trends |  |
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| 2023 | Annette Rogge-Toehgiono | Use of digital technologies in healthcare: approvals in the borderline area between medical device and medical aid – investigation and evaluation of regulatory chances and challenges - medical software applications *** |
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| 2023 | Deanna Yuching Balakhonova | An Overview of Current Regulatory Environment Regarding Artificial Intelligent (AI)-Based Medical Device Software (MDSW) in EU | |
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| 2023 | Dr. Irina Anusca | Clinical Evaluation of light-cure resin modified Dental Composite according to MDR 745/2017 | |
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| 2023 | Dr. Olga Petina | Comparative analysis of the EU regulatory requirements for essential oils as ingredients for the pharmaceutical, cosmetic products and feed additives *** |
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| 2023 | Kay Pötzsch | "The Fair Minimum": Wie deutsche Arzneimittelproduktinformation geschlechtsneutral werden kann
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