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:
https://www.forum-institut.de/seminar/2012233-projektmanagement-in-regulatory-affairs

(Conference organized by FORUM Institut)

HORN Pharmaceutical Consulting
CMC – GMP – Regulatory Affairs
Dr. Hiltrud Horn
Am Alten Schloß 1
D-76646 Bruchsal
Germany

Phone: +49 (0) 7251/305 527
Fax: +49 (0) 7251/305 528
Mobile: +49 (0) 160/5834 213
e-mail: info@horn-pharma.de
Internet: www.horn-pharma.de