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Regulatory
Manufacturing
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R&D
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Legislation
Legislation
Proposed simplification of the MDR and IVDR regulations
Giuliana Miglierini
-
29 January 2026
EFPIA’s report on AI across the medicines lifecycle
staff
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22 December 2025
EPO, a map of specialised investors and free flow of data...
Manuele Cantù
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24 April 2025
Request for an urgent EU Critical Chemicals Act
Giuliana Miglierini
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10 April 2025
Reactions to the Critical Medicines Act
Manuele Cantù
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3 April 2025
EU consultation on medical device legislation
Giuliana Miglierini
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9 January 2025
EFPIA’s white paper on circular economy
Manuele Cantù
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4 June 2024
EU Parliament approved amendments to review of pharmaceutical legislation
Manuele Cantù
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22 April 2024
The JURI Committee position on Union compulsory licensing
Manuele Cantù
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11 April 2024
MedTech Europe comments the political agreement on the PLD directive
Manuele Cantù
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11 January 2024
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