Principles, Procedures, Application Types and Maintenance
Webcode 26122644
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.
anytime
anytime
online
online
Event - 390€ plus tax
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.
SPECIAL OFFER
Outsourcing & Vendor Oversight in Regulatory Affairs
01/10/2026, online
Your booking advantage: You book the seminar at the regular price and add the e-learning. The price of the e-learning is reduced by 100 € to
590,00 €
Event - 390€ plus tax
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.
SPECIAL OFFER
Outsourcing & Vendor Oversight in Regulatory Affairs
01/10/2026, online
Your booking advantage: You book the seminar at the regular price and add the e-learning. The price of the e-learning is reduced by 100 € to
590,00 €
Jean-Marie Bayhurst
Conference Manager
+49 6221 500-685
j.bayhurst@forum-institut.de
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...).
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 revised in 2025.
Dr. Christian M. Moers
Dr. Christian M. Moers
Dr. Christian M. Moers
Dr. Christian M. Moers
Dr. Christian M. Moers
Here you can get a brief insight into the e-Learning Introduction to EU Marketing Authorisation.
Would you like a deeper dive into the RA topic? Check out our course "Regulatory Affairs Starter Pack". Three e-Learning programmes in one bundle: Get a solid foundation in EU marketing authorisation procedures, the EU variation system and the Common Technical Document (eCTD). Your fast track into EU Regulatory Affairs - at a special bundle price.
For more information and registration simply click on this link: Regulatory Affairs Starter Pack
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.
Modules
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Watch the trailer for our e-Learning programme "Introduction to EU Marketing Authorisation".
Details
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Three e-Learning programmes in one bundle. Your fast track into EU Regulatory Affairs!
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