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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| 2004 | Claudia Hettenkofer | Implementation of an internal Standard Operating Procedure for the Preparation of Mutual Recognition Variations *** |
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| 2004 | Dr. Beate Preuss | Quality related changes during the life-cycle of a medicinal product marketed in the EU and their impact on the pharmaceutical documentation (CTD module 3) | |
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| 2004 | Dr. Jan Richter | Scientific and regulatory concepts for the development of molecular targeted anti-cancer drugs *** |
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| 2004 | Anja Kirsten Schiefer | Comparison of the requirements in the registration and marketing authorisation procedure of human homoeopathic medicinal products within the EU with regard to specific requirements in Germany, Austria, the Netherlands and Switzerland as a Non-EU-country *** |
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| 2004 | Dr. Elmar Hermann Schmitt | Regulatory background in the development of medicinal products for human use produced by transgenic animals - current situation in the EU and USA *** |
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| 2004 | Verena Stumpf | Switch from CFC-containing to CFC-free metered dose inhalers - current status and regulatory aspects *** |
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