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

  • 10.11.2022
    Verunreinigungen in Arzneimitteln - Fokus Nitrosamine
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  • 15.11.2022
    MEGRA StartUp
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  • 18.11.2022
    Online Seminar: ATMPs: Quality and risk management
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News

  • 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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  • 25.08.2022
    Important Aspects to consider if you use Titanium Dioxide in your Drug Products
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