FORUM · Institut für Management GmbH
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Online training Educational Material
Educational material
in Europe
2019-08-23 2019-08-23 Online Online

Educational material in Europe

Germany - Netherlands - France - Switzerland - Italy

Educational material will remain a national issue in each European country. Familiarise yourself with the regulations in the Netherlands, France, Switzerland, Italy and Germany in this webcast series consisting of six webcasts.
  • Legal basis in specified European countries
  • Submission to local authorities
  • Distribution of educational material
  • Approval process and timelines
  • Effectiveness indicators
  • The organisational process in your company

Aims and objectives

Educational material in Europe is becoming increasingly important. Therefore, the European Union has published appropriate guidelines. This webcast series shows how some Central European countries have implemented them. The various experts explain the specific recommendations, formats, layouts, timelines and issues that should be considered. The series starts with the PRAC recommendation for health authorities to publish educational material or an indication for a product, and proceeds with the steps a marketing authorisation holder has to follow to fully comply with EU regulations and local legislation.
Who should attend
This webcast series will be of benefit to those working in the European pharmaceutical industry as well as those involved in the preparation and organisation of educational material in the various European countries. Basic knowledge of risk minimisation measures is advantageous.
Your experts
Dr. Thomas Grüger
-requested- Senior Expert Pharmacovigilance, Bonn, Germany

Dr Delphine Bertram
Xendo B.V. - A ProPharma Group Company, Leiden, The Netherlands

Dr. René Haltiner
Senior Process Governance Manager, Novartis Campus, Basel, Switzerland

Hanneke Dominicus
Xendo B.V. - A ProPharma Group Company, Leiden, The Netherlands

Go forward

Our international course portfolio

Our international course portfolio

Are you interested in our international continuous education programme? We provide a variety of specialised courses.


Abbreviations, Glossary

List of abbreviations

Many abbreviations for processes, documents and authorities, amongst others, are used in all regulatory areas. We have compiled the most important ones for you. Our list of abbreviations can be freely downloaded here.


More on our quality criteria

Quality guaranteed!

IMI (Innovative Medicines Initiative) defined quality criteria for professional training and education. We follow these criteria and, as a signatory, we are an active partner in further developing and optimising the quality standards.

An aggregate evaluation of participants' feedback on all FORUM's healthcare training courses (evaluation period from 10.2017 - 09.2018) produced a result of 1.6 (based on a school grading system of 1-6).