2025-07-03 2025-07-03 , online online, 390 € zzgl. MwSt. Dr. Christian M. Moers https://www.forum-institut.de/seminar/25122644-e-learning-introduction-to-eu-marketing-authorisation/referenten/25/25_12/25122644-e-learning-introduction-to-eu-marketing-authorisation_moers-christian-m.jpg e-Learning: Introduction to EU Marketing Authorisation

This e-learning programme will familiarise you with the regulatory affairs principles involved in applying for a marketing authorisation in Europe (MRP, DCP, CP) . It will also introduce you to post-authorisation duties (renewal, variation...).

Topics
  • Module 1: Overview of the law and EU regulatory network
  • Module 2: Principles (The European Economic Area & the scope of Directive 2001/83/EC)
  • Module 3: Procedures (MRP, DCP, CP, Referrals)
  • Module 4: Application types (legal basis, CTD requirements, Generics, Herbals)
  • Module 5: Post authorisation (Renewals, Sunset Clause, Variations)


Who should attend
Do you need basic regulatory affairs expertise since you already work in the pharmaceutical industry or plan to start working in this field? Then this e-Learning programme is the fast track to becoming knowledgeable in this field. No prior regulatory experience is required.
Aims and objectives
This e-Learning programme will familiarise you with the regulatory affairs principles involved in applying for a marketing authorisation in Europe. It addresses the EU marketing authorisation procedures for the various products. It will also introduce you to post-authorisation duties.

Upon completion, you will be conversant with the key principles of regulatory affairs and have a good starting basis to work in this field.

This e-Learning was developed in May 2018 and revised in 2025.
Your benefit

  • Up-to-date expert knowledge & fl exibility in location and timing
  • You will gain an overview of the law and EU regulatory network
  • Get to know the differnt application types and post authorisation procedures
  • Options to test your knowledge and personal certificate
  • All on an intuitive learning platform

e-Learning: Introduction to EU Marketing Authorisation

Introduction to EU Marketing Authorisation

e-Learning

Benefits
  • Up-to-date expert knowledge
  • Flexibility in location and timing
  • You establish your own learning speed
  • Tests and feedback
  • Certificate of completion
  • Compatibility with mobile devices

Webcode 25122644

Jetzt buchen

JETZT Buchen
Referent

Dr. Christian M. Moers

Sträter Lawyers, Bonn, GERMANY

Lawyer; His prime interests are the interdisciplinary challenges of medicinal product law. His focal advisory areas are as follows: - European and German medicinal product law - Marketing authorisation law & regulatory affairs - Pharmacovigilance - Wholesale trade with medicinal products, distribution of medicinal products - Manufacture of medicinal products
More information please click here.

Alles auf einen Blick

Termin

anytime

anytime

Zeitraum

Veranstaltungsort

online

online

Downloads
Gebühr

Veranstaltung - 390 € zzgl. MwSt.
The fee for a single account that is valid for 90 days is €390 (excluding German VAT). You can access the modules as often as you want during this time. You will be awarded a certificate of completion at the end.

Veranstaltung - 390 € zzgl. MwSt.
The fee for a single account that is valid for 90 days is €390 (excluding German VAT). You can access the modules as often as you want during this time. You will be awarded a certificate of completion at the end.

Inhouse-Angebote
Inhouse-Angebot anfordern
Inhouse-Angebot anfordern

Jetzt buchen

Your contact

Jean-Marie Bayhurst
Conference Manager

+49 6221 500-685
j.bayhurst@forum-institut.de

Details

This e-learning programme will familiarise you with the regulatory affairs principles involved in applying for a marketing authorisation in Europe (MRP, DCP, CP) . It will also introduce you to post-authorisation duties (renewal, variation...).

Topics

  • Module 1: Overview of the law and EU regulatory network
  • Module 2: Principles (The European Economic Area & the scope of Directive 2001/83/EC)
  • Module 3: Procedures (MRP, DCP, CP, Referrals)
  • Module 4: Application types (legal basis, CTD requirements, Generics, Herbals)
  • Module 5: Post authorisation (Renewals, Sunset Clause, Variations)


Who should attend
Do you need basic regulatory affairs expertise since you already work in the pharmaceutical industry or plan to start working in this field? Then this e-Learning programme is the fast track to becoming knowledgeable in this field. No prior regulatory experience is required.

Aims and objectives

This e-Learning programme will familiarise you with the regulatory affairs principles involved in applying for a marketing authorisation in Europe. It addresses the EU marketing authorisation procedures for the various products. It will also introduce you to post-authorisation duties.

Upon completion, you will be conversant with the key principles of regulatory affairs and have a good starting basis to work in this field.

This e-Learning was developed in May 2018 and revised in 2025.

Your benefit

  • Up-to-date expert knowledge & fl exibility in location and timing
  • You will gain an overview of the law and EU regulatory network
  • Get to know the differnt application types and post authorisation procedures
  • Options to test your knowledge and personal certificate
  • All on an intuitive learning platform

Programm

Dr. Christian M. Moers

Module 1: Overview of the law and EU regulatory network
  • European Union law
  • National law
  • Soft law
  • EU regulatory network
After having passed this module you can destinguish in between binding law and soft law and understand the principles of the European regulatory network.

Dr. Christian M. Moers

Module 2: Principles
  • Why marketing authorisations?
  • The European Economic Area (EEA)
  • What is a medicinal product?
  • Scope of Directive 2001/83/EC
After having passed this module you

Dr. Christian M. Moers

Module 2: Principles
  • Why marketing authorisations?
  • The European Economic Area (EEA)
  • What is a medicinal product?
  • Scope of Directive 2001/83/EC
After having passed this module you understand the scope of Directive 2001/83/EC. You know under which conditions a product needs a marketing authorisation.

Dr. Christian M. Moers

Module 3: Procedures
  • National ("one-member-state") procedure
  • Mutual recognition procedure (MRP)
  • Decentralised procedure (DCP)
  • Referrals
  • Centralised procedure (CP)
  • Conditions
After having passed this module you understand the marketing authorisation pathways in the EU and know which product is eligable to which procedure.

Dr. Christian M. Moers

Module 4: Application types
  • Dossier
  • Legal basis
  • Generics
  • Data exclusivity
  • Homeopathic and herbal medicinal products
After having passed this module you understand the legal basis for each group of drugs and know which data has to be submitted to the authorities when applying for a marketing authorisation.

Dr. Christian M. Moers

Module 5: Post authorisation
  • Renewals
  • Sunset clause
  • Variations
After having passed this module you know your duties in the drug lifecyle management and understand the variations system.

Trailer

e-Learning: Introduction to EU Marketing Authorisation

Here you can get a brief insight into the e-Learning Introduction to EU Marketing Authorisation.

Principles

Content

The e-learning programme 'Introduction to EU Marketing Authorisation' comprises five didactic modules that include videos in which the expert Dr Christian Moers shares his expertise with you. You can also download and print the corresponding presentation documents.

Each module comprises additional documents (links, guideline texts, etc.) as well as interactive exercises and questions, which help you practise and apply your newly gained knowledge.

Once you have completed the five modules and passed a final multiple-choice test, you will be awarded a certificate, which you can print out directly. The e-learning programme should be completed within three months. Try our e-learning programme for free and familiarise yourself with our learning environment.

How does it work?

1. Register for an e-learning programme on our website.

2. You will receive an email with your login data for our learning platform.

3. Log in to start your e-learning programme.

4. Complete your e-learning modules at your own pace.

5. Finalise the modules with a multiple-choice test.

6. Once you have successfully completed the test, you will be awarded a certificate, which you can print out.

Please try out the demo versions of our e-learning programmes free of charge to get an idea of our learning environment.

This distinguishes our events

Modules

Hour access to your personal learning environment on every day

Recommendations

e-Learning: Grundzüge des deutschen Gesundheitssystems

Hochwertiges e-Learning für Ihren fundierten und flexiblen Einstieg in die Grundzüge des deutschen Gesundheitssystems (P...

31.12.2025 in
Details

e-Learning: AMNOG kurz und knapp

In 5 Modulen HTA-Konzept, Datenanforderungen für das Nutzendossier und Ablauf des AMNOG-Verfahrens bis zur Preisverhandl...

31.12.2025 in
Details

Blitzlicht: Update Kosmetikrecht

Neue Webcast-Serie: Holen Sie sich vierteljährlich ein Rechtsupdate bezüglich kosmetischer Mittel

01.11. - 31.10.2026 in
Details

PharmaFORUM Webcast International

Our global and local experts will update you every two months with the latest regulatory and legislative developments. T...

01.11. - 31.10.2026 in
Details

Online Pharma FORUM

Das Online PHARMA FORUM bietet seit vielen Jahren die Möglichkeit, sich einmal pro Monat über das Internet in den Themen...

01.12. - 30.11.2026 in
Details

Go forward

Trailer

Watch the trailer for our e-Learning programme "Introduction to EU Marketing Authorisation".

Details
Trailer e-Learning
e-Learning - Click and learn

The FORUM · Institut für Management GmbH provides flexible education and training with high-quality e-Learning programme...

Details
e-Learning
We guarantee the highest quality

We are now officially certified to ISO 9001 and ISO 21001 standard.

Details
We guarantee the highest quality