13.03.2018
Mannheim: Die FDA nach dem MRA: Grundlagen und aktuelle Entwicklungen (QS 3)
In this conference, Dr. Hiltrud Horn will give detailed insight into the essentials about regulatory requirements in US and preparation of dossiers in US (IND, NDA, DMF). Furthermore Dr. Horn will present how to successfully prepare for meetings with Authorities and how to handle changes.
For more information please visit the following website:
https://www.gmp-navigator.com/daten/seminarpdf/QS3-Die-FDA-nach-dem-MRA.pdf
(Conference organized by Concept Heidelberg)
Back 