Opportunity Information: Apply for PAR 18 885
The grant opportunity titled "Novel Approaches to Safe, Non-Invasive, Real Time Assessment of Human Placenta Development and Function Across Pregnancy (R21 - Clinical Trial Not Allowed)" is a National Institutes of Health (NIH) funding announcement that supports early-stage, exploratory research aimed at improving how clinicians and researchers can monitor the human placenta during pregnancy. The central goal is to spur the development of new methods that can assess placental development and function in vivo, in real time, using approaches that are safe and non-invasive, or at least minimally invasive. In practical terms, the FOA is looking for tools, technologies, or measurement strategies that could track placental health and performance across the full course of pregnancy, rather than relying on indirect or late-stage indicators that often appear only after complications have progressed.
This is an R21 mechanism, which typically emphasizes innovation and proof-of-concept work rather than large, fully scaled clinical validation programs. The announcement explicitly states "Clinical Trial Not Allowed," meaning applicants should not propose studies that meet the definition of a clinical trial (for example, prospectively assigning human participants to an intervention to evaluate health-related outcomes). Projects can still involve human subjects when appropriate, but the work needs to remain within non-trial boundaries, such as technology development, feasibility testing, observational data collection, or validation work that does not involve interventional assignment in the clinical-trial sense. The intent is to get promising ideas off the ground and generate foundational evidence that could justify more extensive follow-on studies under other mechanisms.
From a funding and administrative standpoint, this opportunity is categorized as a discretionary grant within the federal Health, Income Security and Social Services activity area and is associated with CFDA number 93.865. The opportunity number is PAR-18-885, and it was created on 2018-08-01, with an original closing date listed as 2021-12-06. The listed award ceiling is $200,000, signaling that NIH expects relatively modest budgets consistent with an exploratory R21 scope. While the source text does not provide a specific number of expected awards, the ceiling gives applicants a clear sense of the scale of work NIH expects: focused, high-impact, and technically ambitious, but not a multi-site, long-duration clinical effort.
A major theme of this FOA is the emphasis on real-time assessment of the placenta across pregnancy. That framing matters because placental disorders and dysfunction can evolve dynamically, and many existing clinical approaches provide limited insight into placental biology until problems become severe. By encouraging real-time, in vivo measurement, the FOA is pushing the field toward methods that can capture placental changes as they occur, potentially enabling earlier detection of dysfunction and a better understanding of pregnancy complications linked to placental development and performance. The "non-invasive (or minimally invasive)" requirement highlights safety and feasibility in pregnant populations, where risk tolerance is necessarily low and repeated measurements over time are often essential.
Eligibility is broad and includes a wide range of U.S. and non-U.S. entities. Eligible applicants listed 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 and Indian housing authorities; nonprofits both with and without 501(c)(3) IRS status (as long as they are not institutions of higher education in that category); for-profit organizations other than small businesses; and small businesses. The FOA also explicitly names additional eligible applicant types such as Alaska Native and Native Hawaiian Serving Institutions, AANAPISI institutions, Hispanic-serving institutions, historically Black colleges and universities (HBCUs), tribally controlled colleges and universities (TCCUs), faith-based or community-based organizations, eligible federal agencies, U.S. territories or possessions, and non-domestic (foreign) entities as well as regional organizations. This wide eligibility suggests NIH is interested in attracting ideas from traditional academic labs, technology developers, community-connected organizations, and international groups that may bring unique measurement capabilities or perspectives.
Overall, the opportunity is designed to accelerate innovation in placental monitoring by funding the creation and early demonstration of new measurement approaches that are safe for pregnancy and capable of providing real-time information on placental development and function. The R21 structure and the clinical-trial restriction together signal that NIH wants high-risk, high-reward methodological advances and feasibility evidence, setting the stage for later-stage translational work that could eventually improve clinical monitoring and outcomes related to placental health.Apply for PAR 18 885
- The National Institutes of Health in the health, income security and social services sector is offering a public funding opportunity titled "Novel Approaches to Safe, Non-Invasive, Real Time Assessment of Human Placenta Development and Function Across Pregnancy (R21 - Clinical Trial Not Allowed)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.865.
- This funding opportunity was created on 2018-08-01.
- Applicants must submit their applications by 2021-12-06. (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 $200,000.00 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.
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Frequently Asked Questions (FAQs)
What is the title of this grant opportunity?
The opportunity is titled "Novel Approaches to Safe, Non-Invasive, Real Time Assessment of Human Placenta Development and Function Across Pregnancy (R21 - Clinical Trial Not Allowed)."
Which agency is offering this funding opportunity?
This is a National Institutes of Health (NIH) funding announcement.
What is the main purpose of this funding announcement?
The main purpose is to support early-stage, exploratory research that improves how clinicians and researchers can monitor the human placenta during pregnancy by developing new ways to assess placental development and function in vivo and in real time, using approaches that are safe and non-invasive (or at least minimally invasive).
What kinds of projects is this FOA trying to encourage?
The FOA is encouraging tools, technologies, or measurement strategies that can track placental health and performance across the full course of pregnancy, rather than relying on indirect measures or signs that only show up after complications have progressed.
What does "real-time assessment" mean in the context of this opportunity?
Within this opportunity, "real-time" refers to methods designed to capture placental changes as they occur during pregnancy, allowing monitoring across time rather than only providing limited or delayed insights into placental biology.
Why does the FOA emphasize monitoring across the full course of pregnancy?
The FOA highlights that placental disorders and dysfunction can evolve dynamically. Monitoring across pregnancy is intended to help capture these changes over time and potentially enable earlier detection of dysfunction.
What does "safe and non-invasive (or minimally invasive)" mean here?
It means proposed approaches should prioritize safety and feasibility for use in pregnant populations, where risk tolerance is low and repeated measurements over time may be essential.
What funding mechanism is this opportunity using?
This opportunity uses the NIH R21 mechanism, which typically supports early-stage, exploratory, and proof-of-concept research rather than large, fully scaled validation programs.
What does the R21 mechanism imply about the scope of work?
It implies NIH is looking for focused, high-impact, technically ambitious projects that generate foundational evidence and demonstrate feasibility, rather than multi-site, long-duration clinical efforts.
Are clinical trials allowed under this opportunity?
No. The announcement explicitly states "Clinical Trial Not Allowed."
What does "Clinical Trial Not Allowed" mean for applicants?
Applicants should not propose studies that meet the definition of a clinical trial, such as prospectively assigning human participants to an intervention to evaluate health-related outcomes.
Can projects include human subjects even though clinical trials are not allowed?
Yes. Projects can involve human subjects when appropriate, as long as the work stays within non-trial boundaries such as technology development, feasibility testing, observational data collection, or validation work that does not involve interventional assignment in the clinical-trial sense.
What is the central research focus of this FOA?
The central focus is developing novel approaches for in vivo, real-time assessment of human placenta development and function across pregnancy, emphasizing safety and non-invasiveness (or minimal invasiveness).
What type of grant is this categorized as?
It is categorized as a discretionary grant within the federal Health, Income Security and Social Services activity area.
What is the CFDA number associated with this opportunity?
The CFDA number listed is 93.865.
What is the opportunity number?
The opportunity number is PAR-18-885.
When was this opportunity created?
The opportunity was created on 2018-08-01.
What is the original closing date listed for this opportunity?
The original closing date listed is 2021-12-06.
What is the award ceiling for this opportunity?
The listed award ceiling is $200,000.
Does the FOA specify how many awards NIH expects to make?
No. The provided information does not list a specific number of expected awards.
What does the $200,000 award ceiling suggest about project budgets?
It suggests NIH expects relatively modest budgets consistent with an exploratory R21 scope, aimed at feasibility and early demonstration rather than large-scale clinical validation.
Who is eligible to apply?
Eligibility is broad and includes U.S. and non-U.S. entities across government, education, nonprofit, and industry sectors, including but not limited to state/county/local governments, special district governments, independent school districts, public and private institutions of higher education, tribal governments and organizations, public housing authorities, nonprofits with or without 501(c)(3) status (as specified), for-profit organizations (other than small businesses), and small businesses.
Are non-U.S. (foreign) organizations eligible to apply?
Yes. The FOA explicitly includes non-domestic (foreign) entities and regional organizations among eligible applicants.
Are U.S. territories or possessions eligible to apply?
Yes. U.S. territories or possessions are explicitly listed as eligible.
Are faith-based or community-based organizations eligible?
Yes. The FOA explicitly includes faith-based or community-based organizations among eligible applicant types.
Are minority-serving institutions specifically mentioned as eligible?
Yes. The FOA explicitly names Alaska Native and Native Hawaiian Serving Institutions, AANAPISI institutions, Hispanic-serving institutions, historically Black colleges and universities (HBCUs), tribally controlled colleges and universities (TCCUs), and related organizations as eligible.
Why is NIH casting a wide eligibility net for this opportunity?
Based on the description, the broad eligibility suggests NIH is seeking innovative ideas from traditional academic labs, technology developers, community-connected organizations, and international groups that may bring unique measurement capabilities or perspectives.
What is the practical outcome NIH is aiming for through this FOA?
The FOA aims to accelerate innovation in placental monitoring by funding the creation and early demonstration of new measurement approaches that are safe for pregnancy and capable of providing real-time information on placental development and function.
How does this FOA position projects for future funding or follow-on studies?
The R21 structure and emphasis on foundational evidence are intended to get promising ideas off the ground and generate proof-of-concept or feasibility data that could justify more extensive follow-on studies under other funding mechanisms.
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| Novel Approaches to Safe, Non-Invasive, Real Time Assessment of Human Placenta Development and Function Across Pregnancy (R01 - Clinical Trial Not Allowed) Apply for PAR 18 884 Funding Number: PAR 18 884 Agency: National Institutes of Health Category: Health, Income Security and Social Services Funding Amount: Case Dependent |
| Clinical Trial Readiness for Rare Diseases, Disorders, and Syndromes (R21 Clinical Trial Not Allowed) Apply for PAR 18 953 Funding Number: PAR 18 953 Agency: National Institutes of Health Category: Health, Income Security and Social Services Funding Amount: $200,000 |
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