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PRECISE - Improving detection, risk prediction and therapy for inherited heart diseases

Awarded

KICH2.V4P.HS23.100International

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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The PRECISE project is an award-notice initiative managed by the Nederlandse Organisatie voor Wetenschappelijk Onderzoek under the Kennis- en innovatieconvenant. This collaborative effort brings together researchers, companies, patients, and healthcare providers to enhance the quality of care for individuals affected by inherited heart diseases, which impact approximately one in 200 people. The primary objectives of the partnership are to improve early detection within patients and their families, refine risk prediction models, and test innovative therapeutic treatments. Additionally, the project aims to support the development of scientifically sound policies and provide enhanced education and information for both patients and medical practitioners.

General Info

NWO project improving care, detection, and treatment for inherited heart disease patients.

Agency

Nederlandse Organisatie voor Wetenschappelijk Onderzoek → Kennis- en innovatieconvenant

Contract Value

$0

NAICS

541715 - Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)

Place of Performance

Not specified

Set-Aside

NONE

Awardee

Amsterdam UMC - Locatie VUmc

Award Issued Date

04/15/2026, 12:00:00 AM UTC

Documents

0

No documents available

Documents will appear here when they are available.

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Timeline

PhaseAwarded

PostedApr 15

Award Notice

AwardedApr 15

Contract was awarded

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Organization & Contact Information

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AgencyNederlandse Organisatie voor Wetenschappelijk Onderzoek → Kennis- en innovatieconvenant

ContactsNo contacts available

OfficeN/A

Organization / AgencyNederlandse Organisatie voor Wetenschappelijk Onderzoek → Kennis- en innovatieconvenant

Office AddressN/A

ContactsNo contact information available

Full Description

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Ongeveer 1 op de 200 mensen wordt getroffen door een erfelijke hartziekte. Een groep onderzoekers, bedrijven, patiënten en zorgverleners bundelen hun krachten om gezondheidszorg voor patiënten met erfelijke hartziekten te verbeteren. Samen willen zij de vroege detectie van erfelijke hartziekten in patiënten en hun families verbeteren, het risico voor ziekte beter voorspellen, en nieuwe mogelijke behandelingen testen. Verder willen zij bijdragen aan wetenschappelijk verantwoord beleid en aan betere voorlichting en scholing voor patiënten en hun behandelaars die te maken krijgen met erfelijke hartziekten.

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