Opportunity Information: Apply for RFA HL 17 015
Apply for RFA HL 17 015
- The HHS-NIH11 in the health sector is offering a public funding opportunity titled "Bold New Bioengineering Methods and Approaches for Heart, Lung, Blood and Sleep Disorders and Diseases (R21)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.233, 93.837, 93.838, 93.839, 93.840,.
- This funding opportunity was created on Jun 13, 2016 and posted on Jun 13, 2016.
- Applicants must submit their applications by May 10, 2019. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- Each selected applicant is eligible to receive up to $150,000.00 in funding.
- Eligible applicants include: State governments, County governments, City or township governments, Special district governments, Independent school districts, Public and State controlled institutions of higher education, Native American tribal governments (Federally recognized), Public housing authorities/Indian housing authorities, Native American tribal organizations (other than Federally recognized tribal governments), Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education, Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education, Private institutions of higher education, For profit organizations other than small businesses, Small businesses, Others (see text field entitled Additional Information on Eligibility for clarification).
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Opportunity Summary:
Bold New Bioengineering Methods and Approaches for Heart, Lung, Blood and Sleep Disorders and Diseases (R21) (RFA-HL-17-015) is a National Institutes of Health funding opportunity, administered through HHS/NIH (in practice, this aligns with the mission space of the National Heart, Lung, and Blood Institute), aimed at sparking early, high-impact bioengineering research that could change how heart, lung, blood, and sleep disorders are understood, detected, monitored, or treated. The FOA is built around proof-of-concept work, meaning the emphasis is on demonstrating feasibility and generating convincing preliminary evidence that a new engineering-driven method or approach can work, rather than delivering a fully mature product or definitive clinical trial outcomes. It explicitly welcomes projects across the spectrum of basic, translational, and clinical research as long as the proposed work advances bioengineering approaches relevant to these disease areas.
The grant mechanism is an R21, which is typically used by NIH to support exploratory and developmental projects that are novel, potentially transformative, and somewhat higher risk than standard incremental research. In that spirit, this FOA encourages applicants to propose bold methods and enabling technologies, including new tools, platforms, devices, measurement approaches, computational strategies, or engineered systems that can open up previously difficult questions or clinical needs in cardiopulmonary, hematologic, and sleep health. Projects may focus on the creation of new bioengineering techniques, the adaptation of emerging engineering capabilities into these biomedical domains, or the early demonstration that an approach can function in relevant laboratory, animal, or human settings. The key theme is advancement of bioengineering approaches rather than routine hypothesis testing using established methods.
From a funding perspective, the opportunity is categorized as a discretionary grant program, with an award ceiling listed as $150,000. Applicants should treat that ceiling as a practical upper bound for the proposed budget under this announcement and plan a tightly scoped set of aims that can credibly deliver a proof-of-concept outcome within the resource limits. The FOA listing does not specify the number of expected awards in the provided source snippet, but the R21 format generally implies a competitive selection focused on innovation, significance, and feasibility of the proposed concept.
Eligibility is broad and includes a wide range of domestic organization types. Eligible applicants include state, county, and local governments; special district governments; independent school districts; public and state-controlled institutions of higher education; private institutions of higher education; federally recognized Native American tribal governments; other Native American tribal organizations; public housing authorities/Indian housing authorities; nonprofits with or without 501(c)(3) status (excluding institutions of higher education in those specific nonprofit categories); for-profit organizations other than small businesses; small businesses; and other entities as allowed under the FOA’s additional eligibility text. This broad eligibility aligns with the engineering and translational nature of the program, where academic labs, hospitals, nonprofit research centers, and commercial entities may all be positioned to contribute new methods or prototype technologies.
The activity category is Health, and the opportunity is associated with multiple CFDA numbers (93.233, 93.837, 93.838, 93.839, 93.840), reflecting NIH’s cataloging across related institute and program lines that touch heart and vascular disease, lung disease, blood disorders, sleep research, and related translational efforts. The opportunity was posted and created on June 13, 2016, and the closing date for applications was May 10, 2019, indicating it is a past-dated announcement in the form provided. Even so, the described purpose remains useful as a reference point for the kind of work NIH seeks under exploratory bioengineering-focused R21 initiatives in these disease areas.
In practical terms, a strong application under this FOA would typically be expected to clearly identify an unmet need or bottleneck in heart, lung, blood, or sleep disorder research or care, then present an engineering-based approach that is distinctly new or used in a novel way, and finally lay out a realistic plan to demonstrate feasibility. Because the FOA emphasizes proof-of-concept, proposed milestones often center on showing that a prototype can generate interpretable signals, that a new assay can reliably measure a target, that a computational model can predict clinically meaningful outcomes, or that a new interface or device concept can operate safely and effectively in a relevant test environment. The overall aim is to de-risk an innovative bioengineering concept enough that it can later be scaled into larger validation studies, product development, or more definitive clinical research.
Frequently Asked Questions (FAQs)
What is the funding opportunity?
It is an NIH funding opportunity titled Bold New Bioengineering Methods and Approaches for Heart, Lung, Blood and Sleep Disorders and Diseases (R21) with FOA number RFA-HL-17-015. It is administered through HHS/NIH and aligns in practice with the National Heart, Lung, and Blood Institute mission space.
What is the main goal of this FOA?
The goal is to spark early, high-impact bioengineering research that could change how heart, lung, blood, and sleep disorders are understood, detected, monitored, or treated. The emphasis is on bold, enabling engineering-driven methods and approaches rather than incremental studies.
What does "proof-of-concept" mean for this announcement?
Proof-of-concept means the project should focus on demonstrating feasibility and generating convincing preliminary evidence that a new engineering method or approach can work. The FOA is not centered on delivering a fully mature product or producing definitive clinical trial outcomes.
What grant mechanism is used and what does it imply?
This FOA uses the NIH R21 mechanism, which typically supports exploratory and developmental projects that are novel, potentially transformative, and somewhat higher risk than standard incremental research. The expectation is a tightly scoped, innovative project designed to de-risk a new concept.
What research areas does this opportunity cover?
It covers bioengineering methods and approaches relevant to heart, lung, blood, and sleep disorders and diseases. Projects can address how these conditions are understood, detected, monitored, or treated, as long as the work advances a bioengineering approach.
Is the FOA limited to basic research, or can it include translational and clinical work?
It explicitly welcomes projects across the spectrum of basic, translational, and clinical research, as long as the proposed work advances bioengineering approaches relevant to the covered disease areas.
What types of projects are encouraged?
The FOA encourages bold methods and enabling technologies, including new tools, platforms, devices, measurement approaches, computational strategies, or engineered systems. Projects may involve creating new techniques, adapting emerging engineering capabilities to these biomedical domains, or demonstrating early functionality in relevant settings.
What kinds of technologies or approaches are specifically mentioned as examples?
Examples described include new tools, platforms, devices, measurement approaches, computational strategies, and engineered systems that help address previously difficult questions or clinical needs in cardiopulmonary, hematologic, and sleep health.
What is the key theme reviewers would likely look for based on the description?
The key theme is the advancement of bioengineering approaches rather than routine hypothesis testing using established methods. The project should be distinctly new or use an existing engineering approach in a novel way for these disease areas.
What is the award ceiling mentioned for this opportunity?
The opportunity is described as a discretionary grant program with an award ceiling listed as $150,000. Applicants are advised to treat this as a practical upper bound for the proposed budget and to scope aims accordingly.
Does the provided information state how many awards will be made?
No. The provided snippet does not specify the expected number of awards. It does note that the R21 format generally implies a competitive selection focused on innovation, significance, and feasibility.
Who is eligible to apply?
Eligibility is broad and includes many domestic organization types, including governments, higher education institutions, tribal entities, nonprofits, and for-profit organizations (including small businesses), as described in the FOA summary.
Which government entities are eligible?
Eligible government applicants include state, county, and local governments, as well as special district governments.
Are educational institutions eligible?
Yes. Eligible applicants include independent school districts, public and state-controlled institutions of higher education, and private institutions of higher education.
Are tribal organizations eligible?
Yes. Eligible applicants include federally recognized Native American tribal governments and other Native American tribal organizations.
Are housing authorities eligible?
Yes. Public housing authorities/Indian housing authorities are listed among eligible applicants.
Are nonprofits eligible, and does 501(c)(3) status matter?
Yes. Eligible applicants include nonprofits with or without 501(c)(3) status (excluding institutions of higher education within those specific nonprofit categories, as stated in the provided eligibility description).
Are for-profit organizations eligible?
Yes. Eligible applicants include for-profit organizations other than small businesses as well as small businesses.
What is the activity category for this opportunity?
The activity category is Health.
Which CFDA numbers are associated with this opportunity?
The opportunity is associated with multiple CFDA numbers: 93.233, 93.837, 93.838, 93.839, and 93.840.
What do the multiple CFDA numbers indicate?
They reflect NIH cataloging across related institute and program lines that touch heart and vascular disease, lung disease, blood disorders, sleep research, and related translational efforts.
When was the opportunity posted and when did it close?
The opportunity was posted and created on June 13, 2016, and the closing date for applications was May 10, 2019.
Is this an active funding opportunity based on the dates provided?
Based on the provided dates, it appears to be past-dated in the form shown (closing date May 10, 2019).
What kind of project plan would typically fit the "tightly scoped" R21 expectation described?
A fit-for-purpose plan would identify an unmet need or bottleneck in heart, lung, blood, or sleep research or care, propose a distinctly new engineering-based approach, and lay out a realistic set of steps to demonstrate feasibility within the resource limits and proof-of-concept focus.
What are examples of proof-of-concept milestones mentioned or implied in the description?
Milestones often center on demonstrating that a prototype can generate interpretable signals, that a new assay can reliably measure a target, that a computational model can predict clinically meaningful outcomes, or that a new interface or device concept can operate safely and effectively in a relevant test environment.
What settings can be used to demonstrate feasibility?
The description indicates feasibility can be demonstrated in relevant laboratory, animal, or human settings, depending on the approach.
What is the intended next step after a successful proof-of-concept under this FOA?
The aim is to de-risk an innovative bioengineering concept enough that it can later be scaled into larger validation studies, product development, or more definitive clinical research.
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