15.11.2022

MEGRA StartUp

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 learn how to prepare and submit INDs and NDAs and how to handle changes of your marketed products. Use this opportunity to get in-depth insight into the FDA's fundamental concepts. Learn about the importance of regulatory strategies.

For more information please visit the following website:

 (Conference organized by MEGRA)


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Events

  • 27.-28.02.2024
    Online Seminar: APIs in Regulatory Affairs
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  • 19.-20.03.2024
    Online Seminar: Projektmanagement in Regulatory Affairs
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  • 18.-19.06.2024
    Online Seminar: Der Regulatory Affairs Manager
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News

  • 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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