13.-14.11.2019

Mannheim: 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:
https://www.forum-institut.de/seminar/1911230-projektmanagement-in-regulatory-affairs


(Conference organized by FORUM Institut)


Back

HOTLINE

Phone +49 (0) 7251/305 529
Fax +49 (0) 7251/305 528
Mail

Events

Get all events



News

  • 19.12.2022
    EU Update regarding Deadlines of Nitrosamine Impurities
    More
  • 01.09.2022
    EU-GMP Annex 1 finally published
    More
  • 26.08.2022
    New Deadlines and Chances for Nitrosamines
    More
Get all news