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Events 2008
09. - 10.06.2008
Prague: The FDA Organisation, Inspection, Application and Approval
During this two days seminar in Prague, the attendees learnt from Dr. Hiltrud Horn the essentials about regulatory requirements in US and preparation of dossiers in US. Furthermore Dr. Horn presented ...
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23. - 26.06.2008
Dublin: Biopharmaceutical Development and Manufacturing
At this conference, Dr. Hiltrud Horn gave an intensive 1 day training workshop about the regulatory requirements and strategies to be considered for clinical trials, preparation of IMPDs and ...
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22. - 25.07.2008
Mannheim: Certified Regulatory Affairs Manager
On this four days seminar, Dr. Hiltrud Horn gave an intensive three days training course on regulatory requirements in Europe and US. The participants received a detailed insight into all regulatory ...
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28. - 29.08.2008
Cologne: Sichere Zulassung bei der FDA
Dr. Hiltrud Horn gave a two day intensive training in Köln about regulatory requirements in US. On this event, Dr. Horn gave detailed insight into the FDA regulated world. People learnt how to ...
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16. - 17.09.2008
Brussels: Filing Variations 2008
In this two days conference, Dr. Hiltrud Horn gave a presentation on how to deal with change control within a global company. (Conference organized by Informa)
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23. - 26.09.2008
Düsseldorf: Certified Regulatory Affairs Manager
On this four days seminar, Dr. Hiltrud Horn gave an intensive three days training course on regulatory requirements in Europe and US. The participants received a detailed insight into all regulatory ...
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+49 (0) 7251/305 529
+49 (0) 7251/305 528
Events
20.-21.06.2022
Online Seminar: Der Regulatory Affairs Manager
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23.-24.06.2022
Online Seminar: APIs in Regulatory Affairs
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25.08.2022
Online Seminar: Prozessvalidierung - Aktuelle Anforderungen an CMC-Daten
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News
16.05.2022
New Clinical Trials Regulation and new IMPD-Guidelines in place
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29.10.2020
Latest Guidances regarding Nitrosamine Impurities
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18.05.2020
Impact of COVID-19 pandemic on Pharma: GMP and Regulatory Flexibility
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