19.-20.03.2019

Prague: How to write the Quality Part of an IMPD

In this two days conference, Dr. Hiltrud Horn will give detailed insight into the Quality Part of an IMPD. Her presentations on the first day will cover regulatory requirements and challenges of the IMPD. She will provide guidance and advice on the planning, preparation and submission of the IMPD. On the second day you will learn how to efficiently write the Quality section of an IMPD. Furthermore she will present a case study about "Planning of an IMPD". Learn about the changing environment for clinical trials and get prepared for this now.

For more information please visit the following website:
https://www.gmp-navigator.com/daten/seminarpdf/ECA-How-to-write-Quality-Part-IMPD.pdf


(Conference organized by Concept Heidelberg)

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EU: New Variation System in force as of Jan 1, 2010. Filing of variations will be faster, easier, and more flexible. Have you considered that your Change Control System needs to be updated accordingly?
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