Rubrik: europharm
(Treffer aus pharmind, Nr. 12, Seite 1082 (2025))
von Fritschen M | Schmidt L | Ehmann F | Broich K | Vieths S | Hildebrandt M | Stegemann S | Bilanin M
Platform Technologies and Regulatory Sandboxes / A Blueprint for Accelerated Innovation in EU Pharmaceutical Legislation · von Fritschen M, Schmidt, LL.M. F, Ehmann F, Broich K, Vieths S, Hildebrandt M, Stegemann S, Bilanin M · HTW Berlin und DG SANTE European Commission und European Medicines Agency und Bundesinstitut für Arzneimittel und Medizinprodukte und Paul Ehrlich Institut und TUM School of Medicine, BZKF und Leibniz JointLab First in Translation und GSK, on behalf of EFPIA, Vaccines Europe
Platform Technology Regulatory Sandbox EU Pharma Legislation PTMF Patient Innovation The current revision of the EU pharmaceutical legislation represents the most significant reform in over 2 decades. Its goal is to ensure faster, equitable access to innovative medicines for patients while strengthening EU competitiveness through more flexible tools. Two such instruments were featured prominently in the opening session of the Human Medicines Track at the TOPRA Symposium 2025: the concepts of “Platform Technologies” and the “Regulatory Sandbox”. Together, they modernize the EU regulatory framework to accommodate emerging scientific modalities and adaptive innovative pathways (tab. 1). Stage Legal source [ 1 ], ...