Single Source for the Continuation of the Data Management and Coordinating Center (DMCC) for Rare Diseases Clinical Research Network (RDCRN) (U2C Clinical Trial Not Allowed)
ID: 353422Type: Posted
Overview

Buyer

National Institutes of Health (HHS-NIH11)

Eligible Applicants

Public and State Controlled Institutions of Higher Education

Funding Category

Health

Funding Instrument

Cooperative Agreement

Opportunity Category

Discretionary

Cost Sharing or Matching Requirement

Yes

Original Source

https://grants.gov/search-results-detail/353422

Additional Information

http://grants.nih.gov/grants/guide/rfa-files/RFA-TR-24-021.html
Timeline
    Description

    The National Institutes of Health (NIH) is offering a funding opportunity for a single-source cooperative agreement to the Cincinnati Children's Hospital Medical Center (CCHMC) for the continuation of the Data Management and Coordinating Center (DMCC) supporting the Rare Diseases Clinical Research Network (RDCRN). This initiative aims to enhance the diagnosis, management, and treatment of various rare diseases through collaborative, multi-site research, providing essential administrative, data management, clinical research support, and broad dissemination of findings across a network of over 280 institutions. The program emphasizes non-competitive funding due to the significant investment already made in establishing a cohesive infrastructure, with a total funding commitment of $3.5 million over a project period of up to five years. Interested applicants can find more information and guidelines for application submission at the NIH grants website, with the application deadline set for July 22, 2024.

    Point(s) of Contact
    grantsinfo@nih.gov
    Files
    Title
    Posted
    RFA-TR-24-021.html
    The Department of Health and Human Services issues a funding opportunity for a single-source cooperative agreement to the Cincinnati Children's Hospital Medical Center (CCHMC) for the continuation of the Data Management and Coordinating Center (DMCC) supporting the Rare Diseases Clinical Research Network (RDCRN). This initiative aims to enhance diagnosis, management, and treatment of various rare diseases via collaborative, multi-site research. The DMCC will provide essential administrative, data management, research support, and broad dissemination of findings across a network of over 280 institutions. Key features of the program include the integration of cloud computing resources, established data standards based on FAIR principles, and engagement with patient advocacy groups. Through a structured approach involving multiple cores—administrative, data management, clinical research, and engagement—CCHMC will ensure effective collaboration and data accessibility for community stakeholders. The notice emphasizes non-competitive funding, citing the significant investment already made in establishing a cohesive infrastructure. The opportunity includes guidelines for application submission and adherence to specific requirements, such as maintaining eligibility and registrations with relevant federal systems, with a project period of up to five years and a combined funding commitment of $3.5 million from NCATS and NINDS.
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