Translational Neural Devices (R61/R33 - Clinical Trial Optional)
This NIH cooperative agreement funds translational development of therapeutic and diagnostic devices for nervous-system and neuromuscular disorders, covering clinical prototyping, safety testing, a…
- Deadline
- Jan 28, 2027
- Posted
- Oct 29, 2024
- Award amount
- Amount not specified
- Focus areas
- Health
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We’ll email you before Jan 28, 2027 so you have time to apply.
In plain English
This NIH cooperative agreement funds translational development of therapeutic and diagnostic devices for nervous-system and neuromuscular disorders, covering clinical prototyping, safety testing, and small clinical studies. It's aimed at research institutions with device-development capacity, including universities and minority-serving institutions, and involves close NIH staff involvement in project planning. No award amount is specified.
AI-generated summary to help you decide quickly — verify the official eligibility rules before applying.
Who can apply
Other Eligible Applicants include the following: Alaska Native and Native Hawaiian Serving Institutions; Asian American Native American Pacific Islander Serving Institutions (AANAPISISs); Eligible Agencies of the Federal Government; Faith-based or Community-based Organizations; Hispanic-serving Institutions; Historically Black Colleges and Universities (HBCUs); Indian/Native American Tribal Governments (Other than Federally Recognized); Non-domestic (non-U.S.) Entities (Foreign Organizations); Regional Organizations; Tribally Controlled Colleges and Universities (TCCUs) ; U.S. Territory or Possession.
About this grant
The purpose of this Notice of Funding Opportunity (NOFO) is to encourage investigators to pursue translational activities and small clinical studies to advance the development of therapeutic, and diagnostic devices for disorders that affect the nervous or neuromuscular systems. Activities supported in this program include implementation of clinical prototype devices, non-clinical safety and efficacy testing, design verification and validation activities, obtaining an Investigational Device Exemption (IDE) for a Significant Risk (SR) study or Institutional Review Board (IRB) approval for a Non-Significant Risk (NSR) study, as well as a subsequent small clinical study. The clinical study is expected to provide information about the device function or final design that cannot be practically obtained through additional non-clinical assessments (e.g., bench top or animal studies) due to the novelty of the device or its intended use. This NOFO is a milestone-driven cooperative agreement program and will involve participation of NIH program staff in negotiating the final project plan before award and monitoring of research progress.
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