e-Learning
Webcode 23122643
Dr. Christian M. Moers
Sträter Lawyers, Bonn, Germany
Lawyer;
His prime interests are the interdisciplinary challenges of medicinal product law as presented, for example, in the new GDP guidelines, the ATMPs and in data protection and electronic data communication.
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
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.
Our general terms and conditions (dated 1 November 2021) apply and are available upon request. We can send them to you anytime or you can find them on the internet at www.forum-institut.com/t&c. as well as supplementary/different special conditions listed on the event website in individual cases, shall apply.
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.
Our general terms and conditions (dated 1 November 2021) apply and are available upon request. We can send them to you anytime or you can find them on the internet at www.forum-institut.com/t&c. as well as supplementary/different special conditions listed on the event website in individual cases, shall apply.
Dr. Rebekka Bitsch
Conference Manager
+49 6221 500-565
r.bitsch@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 developed in May 2018 and revised in 2020.
Here you can get a brief insight into the e-Learning Introduction to EU Marketing Authorisation.
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
Hour access to your personal learning environment on every day
Die Grundlagen der "Guten klinischen Praxis" - schaffen Sie mit diesem e-Learning eine solide Basis für Ihre Arbeit in k...
This e-Learning programme will provide you with detailed knowledge on the classification, grouping and submission of var...
Do you need know how regarding CTD/eCTD & CMC? Then this e-learning programme is the fast track to becoming knowledgeabl...
