Introduction to the European Union regulatory system and European Medicines Agency for international regulators and non-governmental organisations
Table of contents
Date:
18/09/2017 to 19/09/2017
Location:
European Medicines Agency, London, UK
This two-day awareness session is for international regulators and non-governmental organisations. It gives an insight into the European Union (EU) regulatory system for medicines and the role of the European Medicines Agency (EMA). Insight into the EU system is of prime importance in an increasingly globalised world where worldwide regulators rely on close cooperation. The EU system is one of the most advanced in the world, but it is also one of the most complex. It is based on a network of decentralised agencies in the EU Member States, supported and coordinated by EMA.
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Programme - Introduction to the European Union regulatory system and European Medicines Agency for international regulators and non-governmental organisations (PDF/461.68 KB)
First published: 09/06/2017
Last updated: 10/07/2017 -
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Module 01 - Presentation - Introduction to the EU Regulatory Network: Transparency, Trust and Reliance (PDF/2.31 MB)
First published: 14/11/2017
Last updated: 14/11/2017 -
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Module 04 - Presentation - Specificities of products for veterinary use (PDF/863 KB)
First published: 13/11/2017
Last updated: 13/11/2017 -
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Module 05 - Presentation - Dealing with unmet medical needs and support to innovation (PDF/2.09 MB)
First published: 13/11/2017
Last updated: 13/11/2017 -
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Module 07 - Presentation - Good practice and inspections (PDF/2.65 MB)
First published: 13/11/2017
Last updated: 13/11/2017 -
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Module 10 - Presentation - Stakeholders engagement (PDF/2.22 MB)
First published: 13/11/2017
Last updated: 13/11/2017 -
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Module 11 - Presentation - EMA and international cooperation (PDF/1.11 MB)
First published: 13/11/2017
Last updated: 13/11/2017