Please read this disclaimer (“disclaimer”) carefully before using the Information Management Toolbox website (“website”, “service”) operated by The European Joint Programme on Rare Diseases (“us”, ‘we”, “our”).
The information and the resources available on this website were collated and verified to the best of our abilities. However, we make no warranties as to the accuracy of the content and assume no liability or responsibility for any error or omission in the content.
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The General Pharmaceutical Framework
The EU Commission is preparing a proposal for new legislation (i.e., The General Pharmaceutical Framework) which will impact multiple aspect of drug development in the EU. Modification of the European Agency (EMA) structure and functioning, Rare Disease and Paediatric drug incentives will be affected. The new legislation is expected for the Q4 of 2023 or Q1 of 2024.