Verbesserter Zugang zu Finanzierung, verkürzte Fristen für klinische Studien, gezielte Förderung für strategische Biotechnologie-Projekte und ein Jahr zusätzliche Marktexklusivität für in der EU entwickelte, getestete und hergestellte Biotech-Innovationen: Das sind die Hauptmaßnahmen des gestern in Straßburg vorgestellten Biotech Acts I, der neben der Überarbeitung der EU-Medizinprodukteverordnung (EU-MDR) die Wettbewerbsfähigkeit der EU-Gesundheitsindustrie stärken soll.
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