Q11207 (Q11207): Difference between revisions

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(‎Removed claims)
(‎Changed an Item)
Property / EU contribution
 
4,208,983.49 Czech koruna
Amount4,208,983.49 Czech koruna
UnitCzech koruna
Property / EU contribution: 4,208,983.49 Czech koruna / rank
 
Normal rank
Property / EU contribution
 
168,359.3396 Euro
Amount168,359.3396 Euro
UnitEuro
Property / EU contribution: 168,359.3396 Euro / rank
 
Preferred rank
Property / EU contribution: 168,359.3396 Euro / qualifier
 
exchange rate to Euro: 0.04 Euro
Amount0.04 Euro
UnitEuro
Property / EU contribution: 168,359.3396 Euro / qualifier
 
point in time: 10 January 2020
Timestamp+2020-01-10T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / budget
 
10,525,090.0 Czech koruna
Amount10,525,090.0 Czech koruna
UnitCzech koruna
Property / budget: 10,525,090.0 Czech koruna / rank
 
Normal rank
Property / budget
 
421,003.60000000003 Euro
Amount421,003.60000000003 Euro
UnitEuro
Property / budget: 421,003.60000000003 Euro / rank
 
Preferred rank
Property / budget: 421,003.60000000003 Euro / qualifier
 
exchange rate to Euro: 0.04 Euro
Amount0.04 Euro
UnitEuro
Property / budget: 421,003.60000000003 Euro / qualifier
 
point in time: 10 January 2020
Timestamp+2020-01-10T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Revision as of 00:19, 12 February 2020

Project in Czech Republic financed by DG Regio
Language Label Description Also known as
English
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Project in Czech Republic financed by DG Regio

    Statements

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    4,208,983.49 Czech koruna
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    168,359.3396 Euro
    10 January 2020
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    10,525,090.0 Czech koruna
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    421,003.60000000003 Euro
    10 January 2020
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    39.9899999904989 percent
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    20 April 2017
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    18 April 2020
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    EXBIO Praha, a.s.
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    49°59'0.49"N, 14°30'9.11"E
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    25250
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    Projekt je zaměřen na VaV technologie přípravy specifických fluorescenčních značek, tzv. tandemových fluorochromů, která umožní výrobu skupiny produktů - In vitro diagnostických (IVD) zdravotnických prostředků pro identifikaci maligních, reaktivních a normálních krevních buněk v klinických vzorcích pomocí průtokové cytometrie. Splněním požadavků regulace 21 CFR 820 bude zaručena možnost registrace nových produktů pro klinické aplikace na celosvětových trzích, včetně USA. a. (Czech)
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    Identifiers

    CZ.01.1.02/0.0/0.0/16_083/0010233
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