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PERMIT SIGNED

PERsonalised MedicIne Trials

Total Cost €

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EC-Contrib. €

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Partnership

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Project "PERMIT" data sheet

The following table provides information about the project.

Coordinator
ECRIN EUROPEAN CLINICAL RESEARCH INFRASTRUCTURE NETWORK 

Organization address
address: 5 RUE WATT
city: PARIS
postcode: 75013
website: www.ecrin.org

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country France [FR]
 Total cost 2˙000˙000 €
 EC max contribution 2˙000˙000 € (100%)
 Programme 1. H2020-EU.3.1.6. (Health care provision and integrated care)
 Code Call H2020-SC1-2019-Single-Stage-RTD
 Funding Scheme CSA
 Starting year 2020
 Duration (year-month-day) from 2020-01-01   to  2021-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    ECRIN EUROPEAN CLINICAL RESEARCH INFRASTRUCTURE NETWORK FR (PARIS) coordinator 441˙250.00
2    UNIVERSITE DE PARIS FR (PARIS) participant 302˙500.00
3    EATRIS ERIC NL (AMSTERDAM) participant 297˙500.00
4    UNIVERSITE DU LUXEMBOURG LU (ESCH-SUR-ALZETTE) participant 285˙000.00
5    PARC SANITARI SANT JOAN DE DEU ES (SANT BOI DE LLOBREGAT) participant 203˙750.00
6    ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI IT (MILANO) participant 157˙500.00
7    FEDERAAL KENNISCENTRUM VOOR DE GEZONDHEIDSZORG BE (BRUXELLES) participant 66˙250.00
8    DEUTSCHES ZENTRUM FUER LUFT - UND RAUMFAHRT EV DE (KOELN) participant 57˙500.00
9    FORUM EUROPEEN DES PATIENTS (FPE) LU (LUXEMBOURG) participant 57˙500.00
10    TMF - TECHNOLOGIE UND METHODENPLATTFORM FUR DIE VERNETZTE MEDIZINISCHE FORSCHUNG EV DE (BERLIN) participant 57˙500.00
11    INSTITUTO DE SALUD CARLOS III ES (MADRID) participant 50˙000.00
12    ISTITUTO SUPERIORE DI SANITA IT (ROMA) participant 23˙750.00
13    UNIVERSITE PARIS DESCARTES FR (PARIS CEDEX 06) participant 0.00

Map

 Project objective

Scientific excellence, and acceptance by health authorities of results derived from research on personalised medicine require standards ensuring validity and reproducibility. The objective of PERMIT is to establish, with all relevant stakeholders and invited experts, recommendations ensuring the robustness of personalised medicine trials, which also requires validation of the stratification methods. In a series of workshops participants, partners and selected experts will address the various aspects of methodology, design, data management, analysis and interpretation in personalised medicine research programmes, with the objective to reach consensus and publish recommendations. A mapping of the literature will inventory methodological practice in the various steps of personalised medicine programmes (WP2) and identify needs in terms of standardised methodology. WP3 will address the design of the stratification and validation cohorts, including the issue of the statistical power and the quality of data. WP4 will focus on the use of the stratification algorithms and the robustness the stratification methods. WP5 will address the translational step needed to select treatments to be tested in each of the clusters. WP6 will be dedicated to randomized clinical trials testing treatments in each cluster (including umbrella / basket designs), or comparing the personalised vs. non-personalised approach. Recommendations and publications in scientific journals, a final meeting and webinars will foster adoption and implementation (WP7). The PERMIT consortium is composed of participants: pan-European research infrastructures (ECRIN, EATRIS, ELIXIR-LU/UNILU), funders (DLR), HTAs (KCE, ISCIII), patients (EPF), regulatory (ISS), data protection (TMF) and scientific experts, whereas partners represent stakeholders interested in the quality of evidence generated by personalised medicine research (industry, medicine agencies, ethics committees, funders, journal editors, HTAs, BBMRI).

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The information about "PERMIT" are provided by the European Opendata Portal: CORDIS opendata.

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