Fluorescent marks for use in medical devices (Q11207): Difference between revisions
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(Removed claim: summary (P836): The project is aimed at R & D for the preparation of specific fluorescent marks, so-called tandem fluorochroms, to enable the production of a product group — In vitro diagnostic (IVD) medical devices to identify malignant, reactive and normal blood cells in clinical samples by flow cytometry. Compliance with the requirements of regulation 21 CFR 820 will guarantee the possibility of registering new products for clinical applications in global...) |
(Created claim: summary (P836): The project is focused on R & D technologies for the preparation of specific fluorescent brands, called tandem fluorochromes, which will enable the production of a group of products – In vitro diagnostic (IVD) medical devices for the identification of malignant, reactive and normal blood cells in clinical samples using flow cytometry. Compliance with the requirements of regulation 21 CFR 820 will guarantee the possibility of registration of new...) |
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The project is focused on R & D technologies for the preparation of specific fluorescent brands, called tandem fluorochromes, which will enable the production of a group of products – In vitro diagnostic (IVD) medical devices for the identification of malignant, reactive and normal blood cells in clinical samples using flow cytometry. Compliance with the requirements of regulation 21 CFR 820 will guarantee the possibility of registration of new products for clinical applications in global markets, including USA. a. (English) | |||||||||||||||
| Property / summary: The project is focused on R & D technologies for the preparation of specific fluorescent brands, called tandem fluorochromes, which will enable the production of a group of products – In vitro diagnostic (IVD) medical devices for the identification of malignant, reactive and normal blood cells in clinical samples using flow cytometry. Compliance with the requirements of regulation 21 CFR 820 will guarantee the possibility of registration of new products for clinical applications in global markets, including USA. a. (English) / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / summary: The project is focused on R & D technologies for the preparation of specific fluorescent brands, called tandem fluorochromes, which will enable the production of a group of products – In vitro diagnostic (IVD) medical devices for the identification of malignant, reactive and normal blood cells in clinical samples using flow cytometry. Compliance with the requirements of regulation 21 CFR 820 will guarantee the possibility of registration of new products for clinical applications in global markets, including USA. a. (English) / qualifier | |||||||||||||||
point in time: 22 October 2020
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Revision as of 15:27, 22 October 2020
Project in Czech Republic financed by DG Regio
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Fluorescent marks for use in medical devices |
Project in Czech Republic financed by DG Regio |
Statements
4,208,983.49 Czech koruna
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10,525,090.0 Czech koruna
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39.99 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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The project is focused on R & D technologies for the preparation of specific fluorescent brands, called tandem fluorochromes, which will enable the production of a group of products – In vitro diagnostic (IVD) medical devices for the identification of malignant, reactive and normal blood cells in clinical samples using flow cytometry. Compliance with the requirements of regulation 21 CFR 820 will guarantee the possibility of registration of new products for clinical applications in global markets, including USA. a. (English)
22 October 2020
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Identifiers
CZ.01.1.02/0.0/0.0/16_083/0010233
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