During this two days seminar, the attendees will learn important aspects of drug registration and project management. Dr. Hiltrud Horn will be one of the main speakers. Her talks will focus on project planning, regulatory strategies for EU and US as well as preparation of global dossiers (CTD). In a case study you will learn what needs to be considered for successful planning of an submission (MAA/NDA).

For more information please visit the following website:

http://www.forum-institut.de/fileadmin/scripts/php/downloader/pdf_download.php?downloadid=1311231

(Conference organized by Forum Institut)

Back