20.06.2017
Bonn: IMPD Biotech - Kommende Anforderungen an die Qualitätsdokumentation
Dr. Hiltrud Horn will present the challenges for preparing the Quality part of the IMPD considering latest changes of the regulation for clinical trials. Understand the new process and learn how to avoid pitfalls. You will receive practical advice on successful planning and submitting of your documentation for clinical trials in EU.
For more information please visit the following website:
http://www.forum-institut.de/seminar/1706273-impd-biotech-kommende-anforderungen-an-die-qualitaetsdokumentation
(Conference organized by FORUM Institut
)
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