EU Regulatory Affairs Introductory Training Course

05.06.2024 - 07.06.2024
DAY 1: 09:00 - 17:00
DAY 2: 09:00 - 17:00
DAY 3: 09:00 - 17:00

Dr. Christian Moers und Weitere

Do you need essential European regulatory affairs knowledge? This online training course gives you a compact overview on all important issues. The training course will be entirely held in English.


  • Day 1: Marketing Authorisation procedures in Europe: Legal basis, mutual recognition, decentralised and centralised procedure in detail
  • Day 2: Marketing Authorisation documents: Data for the dossier, key elements and structure of the SmPC and the package leaflet
  • Day 3: Regulatory lifecycle management: Variations, renewals, eCTD and electronic submission

Who should attend

This seminar will be of benefit to all those working in regulatory affairs or in related departments that need essential European regulatory affairs expertise. Basic pharmaceutical knowledge is recommended but not prerequisite.

Aims and objectives

This online introductory training course will inform you about all the important obligations and challenges in regulatory affairs.

You will learn about the different procedures in Europe and about the data and documents required for successful marketing authorisations. Moreover, you will gain practical knowledge about the regulatory lifecycle management for a product and the structure and submission of an electronic dossier.

Book day 1, day 1 and 2 or all three days, according to your needs! A preparatory e-Learning is included in your booking.

Your benefit

In this seminar you will

  • get to know the basic principles for MA procedures in Europe
  • learn about the different procedures in detail
  • know what to have in mind for SmPC and the package leaflet
  • learn about the different modules of the dossier
  • get to know the Variation system and procedures
  • get to know all you need about the electronic submission
  • learn with many practical examples


FORUM Institut für Management GmbH

Sträter Rechtsanwälte
Kronprinzenstraße 20
D-53173 Bonn

Fon +49 (0) 228 93454-0
Fax +49 (0) 228 93454-54



Dr. Christian Moers

Rechtsanwalt Dr. Moers ist seit 2013 Mitglied der Kanzlei und berät pharmazeutische Unternehmen im Bereich der Zulassung und des Vertriebs von Arzneimitteln, Pharmakovigilanz, Großhandel mit Arzneimitteln und Arzneimittelherstellung.