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intime

Prototyping 'intime' - a NINAAT-based self testing platform to detect infectious diseases

Total Cost €

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EC-Contrib. €

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Partnership

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Project "intime" data sheet

The following table provides information about the project.

Coordinator
SELFDIAGNOSTICS DEUTSCHLAND GMBH 

Organization address
address: DEUTSCHER PLATZ 5 D
city: LEIPZIG
postcode: 4103
website: n.a.

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 Germany [DE]
 Project website http://selfdiagnostics.eu/projects
 Total cost 4˙526˙324 €
 EC max contribution 4˙526˙324 € (100%)
 Programme 1. H2020-EU.3.1.3. (Treating and managing disease)
 Code Call H2020-SMEINST-2-2014
 Funding Scheme SME-2
 Starting year 2015
 Duration (year-month-day) from 2015-04-01   to  2019-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    SELFDIAGNOSTICS DEUTSCHLAND GMBH DE (LEIPZIG) coordinator 3˙575˙024.00
2    BIOATLAS OU EE (TARTU) participant 951˙299.00
3    Recon A/S DK (SONDERBORG) participant 0.00

Map

 Project objective

Presented here is the proposal for the project - Homecare test device ‚intime‘ – targeting to bring the first non-instrumented nucleic acid amplification test device onto the market. Market launch will start out with a device for the diagnosis and screening of the sexually transmitted infection Chlamydia trachomatis followed by a multifunctional device including additionally Neisseria gonorrhoeae and Trichomonas vaginalis. This project is the effort of an international consortium of highly professional partners to bring the modular ‚intime’ homecare diagnostic test from a functional model to the final prototype that is ready to be produced and brought to market. SelfD Technologie will lead this consortium and provide the technology for the device, which was already developed and proven to work in a laboratory setting. Now the homecare test will undergo final prototyping with the help of renowned design company wideblue and the experienced injection molding company Recon. This prototype will then be made in a small series production for a thorough analytical and clinical validation that will allow SelfD to apply for the CE mark and introduce the product shortly after the end of the project. The production will be achieved with Recon and the prepared chemical components necessary for the assay will be provided by Bioatlas, a company that SelfD is already engaged in a strategic partnership with. The clinical trial will be executed by the CRO proinnovera and their great experience and connections will ensure a smooth collection of all relevant data. In short, the ‚intime‘ project will propel the novel diagnostic tool for home use onto the market and thus improve healthcare and allow SelfD to launch their first product and position itself as a promising IVD developer.

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

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