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H2020 Collaboratif : Towards the new generation of clinical trials – trials methodology research – 07/04/20

L’appel à projets en bref

  • Individuel ou collaboratif ? Collaboratif
  • Financé et instruit par ? Commission européenne
  • Pour qui ? TPE/PME/Gd Groupe/Académique/Centres de recherche….
  • Pour quel type de projet (maturité/thématique) : Globalization of clinical research, Globalization of clinical research, Data management
  • Quels critères d’éligibilité (les critères principaux si trop de critères) : 3 pays membres, TRL du projet 3-6. Plus d’informations Annexe A, Annexe C
  • Quel montant de financement ? RIA : 4-6 M€
  • Sous quelle forme ? Subvention
  • Sur quelle durée ? 36 – 48 mois (RIA)

Date limite de dépôt des dossiers

07 Avril 2020, 17H

Comment candidater ?

En ligne : : https://ec.europa.eu/info/funding-tenders/opportunities/portal/screen/opportunities/topic-details/sc1-bhc-37-2020

Joindre le cahier des charges de l’appel à projets (à télécharger)

Joindre le dossier de candidature à l’appel à projets (à télécharger)

Mettre un lien vers la page de présentation de l’AAP sur le site du financeurs (BPI, H2020…) :
https://ec.europa.eu/info/funding-tenders/opportunities/portal/screen/opportunities/topic-details/sc1-bhc-37-2020

Scope

Proposals should focus on methodology research and develop innovative solutions to improve the design, conduct and analysis of clinical trials. Proposals should identify and validate methods that will improve the generalizability of evidence generated through differently designed trials, including personalized medicine approaches and combinatorial interventions. In order to draw meaningful conclusions following state of the art of statistical analyses, applicants need to demonstrate access to adequate clinical trial data sets that will be included into the proposed research. 

The proposed methodology should allow sound extrapolation in various subgroups of disease of high public health burden as well as integration of RTC data and post-approval evidence generation. Furthermore, applicants should identify best practices to prevent bottlenecks in execution of clinical trial, including issues related to patient recruitment, adherence and compliance, governance, ethics, sex and gender-based analysis as well as data sharing. The special attention should be put on non-commercial trials, including quantifiable indicators to measure the qualitative improvement in terms of trial management, data processing, and reporting. Whenever relevant, proposals should cover different aspects of training exercises, including hands-on trainings and closer monitoring of the scientific and technical staff involved in the conduct, management and analysis of the trial.

All literature analyses to define the current state of the art in the clinical trial methodology research must be completed at the time of submission of the proposal. Methodology research related to clinical studies exclusively on medical devices is not in the scope of this topic.

Medicen vous accompagne

Medicen vous accompagne dans le montage de votre dossier, vous labellise et vous entraîne à l’oral devant jury. Si vous souhaitez candidater, contactez notre équipe innovation santé à l’adresse projets@medicen.org pour mettre toutes les chances d’obtenir des financements de votre côté.