Ingrid Prieschl
Zwiers Regulatory Consultancy B.V., A ProductLifeGroup Company, Oss, THE NETHERLANDS
Regulatory Consultant
More information please click here.
anytime
anytime
online
online
Event - 490 € plus tax
The fee for a single account that is valid for 90 days is €490 (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.
Event - 490 € plus tax
The fee for a single account that is valid for 90 days is €490 (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.
Jean-Marie Bayhurst
Conference Manager
+49 6221 500-685
j.bayhurst@forum-institut.de
This e-Learning programme will provide you with detailed knowledge on the classification, grouping and submission of variations in the EU.
This e-Learning programme will provide you with detailed knowledge on the classification, grouping and submission of variations in the EU. It includes both procedural and contentual topics.
Upon completion, you will be conversant with the key principles of variation submission and have a good starting basis to work in this field.
This e-Learning was developed in December 2019 and updated June 2025. It covers all relevant updates introduced by Commission Delegated Regulation (EU) 2024/1701.
NEW: bonus material - live recording of a webcast on the electronic submission of variations from December 2024 (German language with English subtitles).
Here you can get a brief insight into the e-Learning EU Variation System & Procedures.
The e-learning programme 'EU Variation System & Procedures' comprises six didactic modules that include videos and interactive elements in which the expert Ingrid Prieschl shares her expertise with you. You can also download and print the corresponding presentation documents.
Each module comprises additional documents (links, guideline texts, etc.), which help you practise and apply your newly gained knowledge.
Once you have completed the six modules, 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.
Upon completing this programme, you will:
Modules
Hours of learning content
Regulatory expectations regarding risk management for pharmaceuticals in (emerging) markets often contend with the strin...
This course offers a deep dive into patient involvement in HTA processes across Europe, with a focus on the UK and Germa...
You will gain actionable insights into global market access strategies, payer evidence requirements, and health economic...
Are you involved in the implementation and ongoing adaptation of the PV system? In this online course you will learn how...
This seminar will focus on AMNOG and JCA dossier preparation as well as the German AMNOG procedure in comparison with th...
Watch the trailer for our e-Learning programme "EU Variation System & Procedures".
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