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Events 2023
21.-22.06.2023
Online Seminar: APIs in Regulatory Affairs
In this training course about the Regulatory Affairs Know-how of Active Pharmaceutical Ingredients (APIs), Dr. Hiltrud Horn will give detailed insight into the specifications and impurity of APIs ...
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28.-29.06.2023
Online Seminar: Der Regulatory Affairs Manager
During this two days seminar, Dr. Hiltrud Horn will give detailed insight into the essentials of Regulatory Affairs. You will learn how to prepare the Quality part of the dossier and how to deal with ...
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24.08.2023
Online Seminar: Prozessvalidierung - Aktuelle Anforderungen an CMC-Daten
In this training course, Dr. Hiltrud Horn will give detailed insight into the new concept of process validation and the essentials to be considered for the CTD. The latest dossier requirements on ...
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14.-15.11.2023
Online Seminar: Projektmanagement in Regulatory Affairs
During this two days seminar, the attendees will learn important aspects of drug registration and project management. Dr. Hiltrud Horn will be one of the main speakers. Her talks will focus on ...
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16.11.2023
CH-Brugg: MEGRA StartUp DRA plus 2023-CH - Modul 12
Blick aus der Schweiz auf das europäische und US-amerikanische Zulassungssystem - In this course, Dr. Hiltrud Horn will focus on the essential regulatory requirements applicable in the US. You will ...
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19.12.2022
EU Update regarding Deadlines of Nitrosamine Impurities
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01.09.2022
EU-GMP Annex 1 finally published
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26.08.2022
New Deadlines and Chances for Nitrosamines
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