{"id":4348,"date":"2025-08-13T15:07:58","date_gmt":"2025-08-13T15:07:58","guid":{"rendered":"https:\/\/benzifoundation.org\/xvii-foresight-training-course-2025\/"},"modified":"2025-08-13T15:07:58","modified_gmt":"2025-08-13T15:07:58","slug":"xvii-foresight-training-course-2025","status":"publish","type":"post","link":"https:\/\/benzifoundation.org\/it\/xvii-foresight-training-course-2025\/","title":{"rendered":"XVII Foresight Training Course \u2013 2025"},"content":{"rendered":"
\n

FROM RESEARCH TO ACCESS: HOW DOES EUROPE SPEED UP THE AVAILABILITY OF MEDICINES FOR UNMET NEEDS?<\/h3>\n<\/div>\n
\n

3 – 4 November, 2025
\nOnline <\/em> <\/h4>\n

La Fondazione Gianni Benzi ha ospitato <\/strong>la XVII edizione del Foresight Training Course (FTC), che si \u00e8 svolta online il 3 e 4 novembre 2025.<\/strong><\/p>\n<\/div>\n

Il corso ha approfondito lo stato attuale e i progressi della ricerca clinica, con particolare attenzione alle esigenze mediche non ancora soddisfatte. Sono state discusse metodologie innovative, sfide regolatorie e il coinvolgimento degli adolescenti negli studi clinici. Inoltre, \u00e8 stato analizzato lo stato dell\u2019arte delle strategie di finanziamento e degli investimenti, considerando gli incentivi pubblici e i fondi pubblico-privati a livello europeo, nazionale e regionale. Sono stati anche affrontati temi legati all\u2019accesso, come gli appalti congiunti, le politiche nazionali, l\u2019HTA e il coinvolgimento dei pazienti nei processi decisionali e di accesso. <\/p>\n

L\u2019evento ha visto la partecipazione di relatori di spicco provenienti dal mondo regolatorio, dal mondo accademico e da altri gruppi di interesse, ed \u00e8 stato gratuito.<\/p>\n

Le registrazioni di tutte le sessioni sono disponibili sul nostro canale YouTube<\/a><\/strong>. Le slide delle presentazioni sono disponibili cliccando sul nome di ciascun relatore: <\/p>\n

Introductory session – How a new Pharmaceutical Legislation could speed up the marketing of medicines for unmet needs in EU<\/strong>
\nFedele (Duccio) Bonifazi, Fondazione Gianni Benzi onlus – <\/em>Welcome<\/a><\/strong>
\nJohn Joseph Borg, Malta Medicines Authority – <\/em>EU Pharmaceutical Law update – What on the table<\/a><\/strong>
\nStefano Marino, DLA Piper – <\/em>How a new Pharmaceutical Legislation could speed up the marketing of medicines for unmet needs in EU<\/a><\/strong>
\nEnrico Costa, Agenzia Italiana del Farmaco – <\/em>How pharma regulation can promote innovation<\/a><\/strong><\/p>\n

Session 1 – Advancements in clinical research<\/strong>
\nLaura Pioppo, European Medicines Agency<\/em> – The current state of the art of clinical research: the ACT-EU initiative<\/a><\/strong>
\nDonato Bonifazi, TEDDY Network<\/em> – ACT-EU initiative for paediatric research<\/a><\/strong>
\nViviana Giannuzzi, Fondazione Gianni Benzi onlus<\/em> – Regulatory acceptability of innovative research methodologies for rare diseases<\/a><\/strong>
\nGiorgio Reggiardo, Clinical Validation from Biopharmaceutical Findings (CVBF)<\/em> – Application of innovative methodologies and technologies: gaps and synergies between US and EU<\/a><\/strong>
\nValentina Jalby, INVENTS Paediatric expert group<\/em> – Showcasing the experience of involving adolescents in European funded projects and reviewing clinical study tools<\/a><\/strong><\/p>\n

Session 2 – Funding and investments for R&D<\/strong>
\nChristina Kyriakopoulou, European Commission<\/em> – Opportunities for R&D on rare diseases and successful collaborations in EU
\nSolange Corriol-Rohou, Consultant<\/em> – Public-private funding<\/a><\/strong>
\nStefano Portolano, Azafaros<\/em>– Where will industry invest?<\/a><\/strong>
\nLucia Ruggieri, Fondazione Gianni Benzi onlus<\/em> – And if the promoter is a not-for profit entity? The lesson from the Paediatric Regulation<\/a><\/strong><\/p>\n

Session 3 – Access to medicines and medical devices in Europe<\/strong>
\nVincenzo Salvatore, Universit\u00e0 degli Studi dell’Insubria<\/em> – EU Joint Procurement: what we learnt from health threats and the proposal for Critical Medicines Act<\/a><\/strong>
\nAnna Ponzianelli, Moderna<\/em> – Updates from the EU HTA Regulation<\/a><\/strong>
\nMichela Gabaldo, Evotec<\/em> – The EU market of innovative medicines for unmet medical needs: where are we going?<\/a><\/strong>
\nFran\u00e7ois Houyez, EURORDIS<\/em> – The patients\u2019 point of view and their involvement in decision-making and access procedures<\/p>\n

\n

Per maggiori informazioni sulle precedenti edizioni del Foresight, clicca qui<\/a>.<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"

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