Dielectric pads for high field MRI

Información del proyecto

MRI PADS

Identificador del acuerdo de subvención: 850506

DOI

10.3030/850506

Proyecto cerrado

Fecha de la firma de la CE 13 Mayo 2019

Fecha de inicio 1 Junio 2019

Fecha de finalización 31 Mayo 2020

Financiado con arreglo a

• EXCELLENT SCIENCE - Future and Emerging Technologies (FET)

Coste total

€ 113 575,00

Aportación de la UE

€ 100 000,00

Coordinado por

MULTIWAVE TECHNOLOGIES AG
Switzerland

CORDIS proporciona enlaces a los documentos públicos y las publicaciones de los proyectos de los programas marco HORIZONTE.

Los enlaces a los documentos y las publicaciones de los proyectos del Séptimo Programa Marco, así como los enlaces a algunos tipos de resultados específicos, como conjuntos de datos y «software», se obtienen dinámicamente de OpenAIRE .

Resultado final

Websites, patent fillings, videos etc. (1)

Website and logo

A website will be established within the first month of implementation and be regularly updated. It will contain three distinct areas: (i) A general part dedicated to the non-specialized public, explaining in simple terms the performances of the MD; (ii) a section with the publications of scientific results and the presentations given at international conferences;(iii) a section to allow clients to order samples.

Documents, reports (7)

Usability tests results

Its describes the result of the tests conducted to prove the manual instruction and the pads are user friendly. Tests are simulations conducted on technicians and volunteers.

Stability report

Its describes the tests carried out to prove the pads are stable over a period of 12 months. Characterizations carried out on the pads produced in WP1 are : performance in a MRI, mechanical strength tests, homogeneity test, permittivity, visual inspections.

Usability report

It describes the usability report on the pads for CE marking. It includes the report as well as the protocols of the tests conducted on technicians and volunteers to prove the instruction manual and pads are users friendly.

Risk Analysis

It describes the risk analysis of the Pads for CE marking and all needed evidence (tests conducted on pads produced in WP1) for its safety.

Clinical evaluation report

It describes the required clinical evaluation protocol for the CE marking of the pads.

Clinical evaluation tests results

It summarizes the results of the tests described in the clinical evaluation report of the WP2

Dissemination report

The findings of the studies will be submitted in a scientific journal. Pads will be presented at international conferences