21. - 22.11.2016
Frankfurt: Projektmanagement in Regulatory Affairs
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 a submission (MAA/NDA). Benefit from the case studies and
avoid pitfalls. In this training course you will understand the typical
challenges that a project manager in regulatory affairs has to face. You
will understand how to select the right strategies
in order to be successful and efficient for your projects. Take the
chance and benefit from the long-term experience of the speakers.
For more information please visit the following website:
http://www.forum-institut.de/pdf/1611230.pdf
(Conference organized by Forum Institut)
Back 