Reissue of PAR-17-045
This Funding Opportunity Announcement (FOA) will support projects that focus solely on development of technologies with the potential to enable acquisition of basic biomedical knowledge. Projects should be justified in terms of technical innovation, and utility for future biomedical impact.
The products of this research will be functioning prototype instruments, methods, synthetic approaches, biological products, etc., characterized adequately to be ready for first application to the type of biomedical research questions that provide the rationale for their development, but application of the proposed technology to specific biomedical questions is considered beyond the scope of the program, should not be included, and would not be funded.
Proof of concept for the technology must have already been demonstrated, but there should still be significant technical challenges. Applications should include preliminary data. Projects that have significant remaining risk but are supported by early feasibility studies might be appropriate for a three-year R01 application with reduced budget to better manage risk and investment. Projects that are well supported by feasibility studies and propose to develop fully functional prototypes might require higher budgets and a four-year duration (five years for Early Stage Investigators). Projects that primarily focus on optimization, hardening, or obvious extrapolations of established technology might be less competitive.
April 12, 2019
Applicants are encouraged to apply early to allow adequate time to make any corrections to errors found in the application during the submission process by the due date.
Conformance to all requirements (both in the Application Guide and the FOA) is required and strictly enforced. Applicants must read and follow all application instructions in the Application Guide as well as any program-specific instructions noted in Section IV. When the program-specific instructions deviate from those in the Application Guide, follow the program-specific instructions.
Applications that do not comply with these instructions may be delayed or not accepted for review.
Support for Early-Stage Technology Development is Critical to Advance Biomedical Research
Biomedical research is enabled and accelerated by the development of advanced technologies. Technology enables science by providing new ways to answer questions, and more importantly, allowing new types of questions to be asked that could not be anticipated in the absence of the enabling technology. New knowledge drives the imperative for new tools, and those tools open new questions, in a mutually reinforcing positive feedback loop that drives science forward.
A study by NIGMS staff in 2015, which included substantial, detailed input from the biomedical research community in response to a Request for Information (NOT-GM-15-118), concluded that there is a significant unmet need for explicit support of early stage technology development, before nascent tools are ready to be applied to untested biomedical research problems. Early stage technology development can be described in two stages: (I) exploratory proof-of-concept research to determine the best approach(es) for a technology development project, and (II) the subsequent research and development that focuses exclusively on creating and validating a working prototype technology before application to untested biomedical problems is possible.
To address the immediate need for funding programs that support early stage technology development, NIGMS developed programs focusing on the two stages described above. This FOA invites projects in Stage II research and development of a working prototype. A companion FOA, PAR-19-254 "Exploratory Research for Technology Development" supports projects in Stage I evaluation of an untested concept.
Defining Characteristics of Focused Technology Research and Development
Appropriateness for this Program
For this FOA, technology refers to tools that enable basic research rather than directly leading to clinical diagnostics or interventions. This includes laboratory instruments and other devices, algorithms and software, chemical reagents and processes or biological molecules or systems that have been modified by human intervention to become research tools that would find use in the biomedical community and have value for solving basic biomedical problems relevant to the IC mission. Further, this FOA calls for innovative, focused technology development predicated on a broad need or challenge in biomedical research that can be described explicitly. This need should be beyond the capability of current technology. The-state-of-the-art technological performance defines a measurable starting point. The proposed improvement of technical performance should be compared to the state of the art which provides the rationale for developing a fundamentally different technology.
Working Prototypes: Projects at this stage of technology development must be supported by preliminary data demonstrating proof of principle, but significant fundamental technical challenges should remain before a working prototype can be developed and validated. These challenges should be substantial enough to require focused effort over a three-to-eight-year period. The prototype should represent a significant advance over the state of the art since this FOA is designed for concepts that are highly innovative. projects supported by this program should not be low risk, incremental improvements to established technologies. The program is intended to support the development of highly innovative technologies that will address significant opportunities to advance biomedical research. The innovation of the proposed projects should be characterized as a significant advance over the state of the art, and the future significance of the enabled biomedical research.
Published and Unpublished Data: Published and preliminary unpublished data that establishes the current state of the art, feasibility, or investigator expertise can be included. Allowable data includes published literature, and unreviewed preprints, protocols, and publicly available research products. Citations in the application to unpublished sources must include DOI and object type as described in NOT-OD-17-050.
No Biological Aims: Applications in response to this FOA that include biological aims would not be funded, but validation against known standards is encouraged. Biomedical relevance is an essential element of NIH research. However, this stage of technology development should not include immediate short-term application of nascent technologies to challenging biomedical research questions because an insistence on explicit linkage to a specific research problem and the immediate demonstration of an immature technology's effectiveness in that context can distort the technology development process. It can also diminish focus on development of genuinely innovative technology in favor of incremental improvements to existing technologies. In the early stages of technology development, insistence on biomedical applications is counterproductive. Therefore, in this program, application to specific biomedical questions in the time frame of the proposed project is considered beyond the scope of the program and should not be included. A technology research and development project in which an untested biomedical problem serves as a test-bed for demonstration of the technology's impact would be too well-developed for this program, and should be the subject of a conventional R01 application to the Parent R01 FOA.
Milestones: A milestone (or intermediate objective) is a defined event, achievement, or important stage that is used to indicate the progress of a project. Milestones should be descriptive of what will be done and when it will be completed. Milestones should lead logically to the final project objectives. The expected outcome from projects funded under this announcement will be the demonstration of a working prototype or tool that has promise for future application to biomedical hypothesis testing.
Validation: Application to well-characterized model systems to assess performance is appropriate at this stage. Applications of the technology should be limited to test systems chosen to facilitate development of the technology. The aims of the project should be focused entirely on the development of the technology. The products of this research will be functioning prototype instruments, methods, synthetic approaches, etc., characterized adequately to be ready for first application to the type of biomedical research questions that provided the rationale for their development.
Relevance of Research Topics for this FOA
Applicants are strongly advised to consult with the Scientific/Research Contact listed in this FOA for guidance on assessing the relevance of applications for this FOA. Technology development for a specific disease and/or organ system, translational research leading to disease diagnosis and intervention, or preclinical and clinical research should be matched to the appropriate Institutes or Centers (ICs). See the List of NIH of Institutes, Centers, and Offices to learn more about specific missions. Also, as indicated in HOLD FOR NOTICE NUMBER, HIV/AIDS-related applications are no longer supported by NIGMS, and accordingly, will not be accepted for review or funding consideration.
Whether a technology is appropriate for a specific NIH IC can be evaluated by the biological significance and utility that would be enabled by the technology. Historical funding of research topics by institute can be identified with the NIH Reporter to identify the historical fit to any NIH institute and study section . It is recommended that applicants contact program staff for IC eligibility. Final determination of application eligibility for this FOA will be based on the full application after submission.
Concepts should be both innovative (represent a significant advance) and novel (not publicly described). The following examples are not appropriate for this FOA: Incremental advance of technology, obvious substitution of one known element for another, technology that has incremental potential to advance biomedical research, combinations of prior elements with additive utility, technologies that are ready for advanced development and validation.
The mission of NIGMS is to support basic research that increases our understanding of basic biological processes and lays the foundation for future advances in disease diagnosis, treatment, and prevention. NIGMS supports research and technology development that is aimed at understanding general principles, mechanisms, and processes through Divisions with diverse interests. NIGMS does not focus on single classes of cells, tissues, organs, or diseases unless they are used as models for elucidating basic principles. Technology development for a specific disease and/or organ system, translational research leading to disease diagnosis and intervention, or preclinical and clinical research may be more appropriate for other ICs.
The mission of NCCIH is to define, through rigorous scientific investigation, the usefulness and safety of complementary and integrative health interventions and their role in improving health and health care. NCCIH supports technologies which will help to elucidate or quantify the important components and/or mechanisms of action of complex interventions relevant to the Center’s mission.
Choosing the Appropriate Biomedical Technology Development Program
Biomedical Technology Research and Development programs are defined by specific criteria that differentiate each stage of technology development. The process of technology research and development can be divided into three domains. The appropriate FOA in each area for applicants is listed. Further information is available at the NIGMS website, Choosing the Appropriate Biomedical Technology Development Program.
(I) PAR-19-254 - Exploratory Research for Technology Development: These projects evaluate high-risk concepts by exploring possible strategies to develop a potential biomedical technology. This is preliminary research that, if successful, should lead to proof-of-concept, or a demonstration of feasibility. These projects are characterized by a high degree of uncertainty regarding the appropriateness and performance characteristics of the technology in question, with no supporting unpublished and/or preliminary data. The project should be responsive to an unmet need or emerging opportunity in biomedical research. Projects that are ready for prototyping or have a fully defined research plan have advanced beyond a stage appropriate for the R21 mechanism and might be better matched to a three-year R01 mechanism with a reduced budget.
(II) This FOA - Focused Technology Research and Development: These projects focus on the further development of a working prototype technology with potential to enable biomedical research. Projects are characterized by innovative research and development, focused on addressing technical challenges that stand in the way of creating an effective research tool. Projects are supported by preliminary data demonstrating feasibility of the approach. The challenge in these projects lies in how the technical challenges will be addressed more than whether the approach is possible. Projects that have significant remaining risk but are supported by early feasibility studies might be appropriate for a three-year R01 application with reduced budget to better manage risk and investment. Projects that are well supported by proof of concept and propose to develop and validate fully functional prototypes might require higher budgets and a four-year duration (five years for Early Stage Investigators). Projects that primarily focus on optimization, hardening, or obvious extrapolations of established technology might be less competitive. Focused Technology research and development projects will stop short of the application of the emerging technology to specific biomedical research problems.
(III) Parent R01: NIH Research Project Grant: These projects are characterized primarily by the iterative coupling of technology development with the application of emerging technologies to biomedical projects that serve as test-beds. These projects combine aims in technology development with challenging biomedical research aims that are positioned to benefit significantly from access to the technology as it matures. In these cases, technology developers benefit significantly from the opportunity to use biomedical research as a proving ground for robustness and for continued development of technologies. Unlike this technology-focused R01 funding announcements, the Parent R01 applications are evaluated for overall impact on the field of interest, rather than the potential utility of a technical project for future biological research. Projects that include both technical advances and biological hypotheses or discovery are appropriate for the Parent R01 funding announcement.
New Investigators and Early Stage Investigators
As part of the Next Generation Researchers Initiative, investigators who have not yet received substantial support from the NIH are encouraged to apply for technology development FOAs and are given extra consideration during review and funding decisions. Among investigators new to the NIH, many meritorious, innovative technologies have been proposed but not all have generated sufficient enthusiasm in review. NIH provides general guidance on how to write your application to allow reviewers to better evaluate the science and merit of your application. In addition, guidance provided in this FOA on grant logic and strategy is based on reviewer critiques of technology development applications.
Grant: A support mechanism providing money, property, or both to an eligible entity to carry out an approved project or activity.
The OER Glossary and the SF424 (R&R) Application Guide provide details on these application types.
The number of awards is contingent upon NIH appropriations and the submission of a sufficient number of meritorious applications.
The scope of the proposed project should determine the project period. The maximum project period is 4 years, 5 for early stage investigators. The grant may be renewed only one time.
Higher Education Institutions
The following types of Higher Education Institutions are always encouraged to apply for NIH support as Public or Private Institutions of Higher Education:
Nonprofits Other Than Institutions of Higher Education
Applicant organizations must complete and maintain the following registrations as described in the SF 424 (R&R) Application Guide to be eligible to apply for or receive an award. All registrations must be completed prior to the application being submitted. Registration can take 6 weeks or more, so applicants should begin the registration process as soon as possible. The NIH Policy on Late Submission of Grant Applications states that failure to complete registrations in advance of a due date is not a valid reason for a late submission.
Program Directors/Principal Investigators (PD(s)/PI(s))
All PD(s)/PI(s) must have an eRA Commons account. PD(s)/PI(s) should work with their organizational officials to either create a new account or to affiliate their existing account with the applicant organization in eRA Commons. If the PD/PI is also the organizational Signing Official, they must have two distinct eRA Commons accounts, one for each role. Obtaining an eRA Commons account can take up to 2 weeks.
For institutions/organizations proposing multiple PDs/PIs, visit the Multiple Program Director/Principal Investigator Policy and submission details in the Senior/Key Person Profile (Expanded) Component of the SF424 (R&R) Application Guide.
This FOA does not require cost sharing as defined in the NIH Grants Policy Statement.
The NIH will not accept duplicate or highly overlapping applications under review at the same time. This means that the NIH will not accept:
The application forms package specific to this opportunity must be accessed through ASSIST, Grants.gov Workspace or an institutional system-to-system solution. Links to apply using ASSIST or Grants.gov Workspace are available in Part 1 of this FOA. See your administrative office for instructions if you plan to use an institutional system-to-system solution.
All instructions in the SF424 (R&R) Application Guide must be followed.
Specific Aims should be focused on the objective of developing an innovative research tool. The project objectives should be to gain new technological knowledge and measure quantitative advances over state-of-the-art technology. Specific Aims should be questions or hypotheses that are necessary and sufficient to connect the work to be performed to the project objectives.
Specific Aims should advance the technical knowledge required to investigate or manipulate biological systems in the service of furthering basic biomedical research that is supported by each IC. Technical advances should be inventive entities or methods that have future utility to broadly advance biomedical research. Examples would include instruments, devices, processes, algorithms, software, chemicals, biomolecules, or cells that have potential value for generating new basic biomedical research. Biomedical knowledge by itself would not be considered a technological advance. Applications submitted under this FOA that include pursuit of a biological hypothesis will not be considered for funding. Applications that are outside the mission of the Institute and would therefore not have utility for future research supported by the appropriate IC will be withdrawn.
In addition to the topics outlined in the SF424 (R&R) Application Guide, the application should describe the potential impact of the tool that will be developed. The possible future impact of the proposed technology must be compelling and clearly articulated. Because this is early stage technology development, the impact need not be immediate. The Significance should describe both the proposed technical advance over the state of the art, and the future biological applications that would be enabled by the new technology. The state-of-the-art technological performance is defined by all available data, and provides a quantitative starting point for the proposed technological improvement. Limitations of the state of the art provide the rationale for developing a fundamentally different technology. Because this is focused technology development with the objective of producing a working prototype, the biomedical impact is not likely to be immediate. Nonetheless, the possible future impact of the proposed technology must be compelling and clearly articulated. The Significance should clearly define the unmet need or emerging research opportunity that will be addressed by the proposed technology and describe its anticipated use for acquisition of biomedical knowledge. The application should explain the potential impact of the technology in the context of biomedical research. The proposed technology must have a well-articulated potential to address both basic biomedical research needs and technical problems that occur broadly across multiple biological systems or diseases. The rationale for the proposed technology development should be explained and should incorporate discussion of the broad opportunity or need that the new technology will address, as well as a discussion of why the approach to be developed has been selected.
In addition to the topics outlined in the SF424 (R&R) Application Guide, the application should describe the nature of the technical opportunity to be exploited or obstacle to be overcome. The rationale for the proposed solution should be explained. The project should be highly innovative. The technology concept should be novel, inventive entities or methods, with potential utility for biomedical research. Innovation could be evaluated by the increment of technical advance over the state-of-the-art, unanticipated technological advance, and/or the potential shift in current biomedical research or approaches.
The application should describe uncertainties underlying the proposed technology development, including risk of failure. A high degree of uncertainty and risk are appropriate in early stage technology development and should be described realistically. Avoid unrealistic, overly optimistic descriptions of the possible outcomes. Straightforward discussion of the challenges and risks inherent in the research plan is encouraged. Describe the desired performance characteristics of the proposed technology and specific measures that will be used to evaluate progress towards achieving those objectives. Objectives and performance measures should be commensurate with the stage of development of the technology and may be very early in the process.
In addition to the topics outlined in the SF424 (R&R) Application Guide, the application should describe those aspects of the experimental approach that are specific to focused technology development. These include the uncertainties underlying the proposed technology research and development including the risk of failure. The Approach should establish a working prototype with substantially improved technical capacities not provided by current tools. The Approach should describe how data will be obtained, analyzed, and interpreted with sufficient rigor to quantitatively assess project outcomes. The prototype performance that would be required to achieve high reward should be identified in the objectives and milestones. While inclusion of untested biological hypotheses will not be funded, validation of technology with well characterized models or gold standard biological samples is encouraged.
Project objectives should represent a significant increment of technical advance compared to the current state of the art. The challenge in these projects lies in how the technical challenges will be addressed more than whether the approach is possible. Objectives and Milestones: The desired characteristics of the technology at the conclusion of the project should be described as end-point objectives, and intermediate objectives or milestones towards that goal should be presented. The end-point milestones and objectives are measurable project performance criteria that, if achieved, would be a significant increment of technical advance over the state of the art. For focused research, risk is expected and milestones might not be reached on a predictable timetable. Nonetheless, measurable milestones should be defined, and it should be stated whether intermediate or end point project performance would be adequate for working prototypes that have utility for testing future biological hypotheses. Describe the desired performance characteristics of the proposed technology and specific measures that will be used to evaluate progress toward achieving those goals. Applications of the technology should be limited to test systems. The research strategy should explain the rationale for the choice of test systems in terms of the desired performance of the technology and how a test system will facilitate development of the technology.
The following modifications also apply:
If you answered “Yes” to the question “Are Human Subjects Involved?” on the R&R Other Project Information form, you must include at least one human subjects study record using the Study Record: PHS Human Subjects and Clinical Trials Information form or Delayed Onset Study record.
Study Record: PHS Human Subjects and Clinical Trials Information
All instructions in the SF424 (R&R) Application Guide must be followed
with the following additional instructions:
Note: Delayed onset does NOT apply to a study that can be described but will not start immediately (i.e., delayed start).All instructions in the SF424 (R&R) Application Guide must be followed.
See Part 1. Section III.1 for information regarding the requirement for obtaining a unique entity identifier and for completing and maintaining active registrations in System for Award Management (SAM), NATO Commercial and Government Entity (NCAGE) Code (if applicable), eRA Commons, and Grants.gov
Part I. Overview Information contains information about Key Dates and times. Applicants are encouraged to submit applications before the due date to ensure they have time to make any application corrections that might be necessary for successful submission. When a submission date falls on a weekend or Federal holiday , the application deadline is automatically extended to the next business day.
Organizations must submit applications to Grants.gov (the online portal to find and apply for grants across all Federal agencies). Applicants must then complete the submission process by tracking the status of the application in the eRA Commons, NIH’s electronic system for grants administration. NIH and Grants.gov systems check the application against many of the application instructions upon submission. Errors must be corrected and a changed/corrected application must be submitted to Grants.gov on or before the application due date and time. If a Changed/Corrected application is submitted after the deadline, the application will be considered late. Applications that miss the due date and time are subjected to the NIH Policy on Late Application Submission.
Applicants are responsible for viewing their application before the due date in the eRA Commons to ensure accurate and successful submission.
Information on the submission process and a definition of on-time submission are provided in the SF424 (R&R) Application Guide.
This initiative is not subject to intergovernmental review.
All NIH awards are subject to the terms and conditions, cost principles, and other considerations described in the NIH Grants Policy Statement .
Pre-award costs are allowable only as described in the NIH Grants Policy Statement.
Applications must be submitted electronically following the instructions described in the SF424 (R&R) Application Guide. Paper applications will not be accepted.
Applicants must complete all required registrations before the application due date. Section III. Eligibility Information contains information about registration.
For assistance with your electronic application or for more information on the electronic submission process, visit How to Apply – Application Guide. If you encounter a system issue beyond your control that threatens your ability to complete the submission process on-time, you must follow the Dealing with System Issues guidance. For assistance with application submission, contact the Application Submission Contacts in Section VII.
All PD(s)/PI(s) must include their eRA Commons ID in the Credential field of the Senior/Key Person Profile Component of the SF424(R&R) Application Package. Failure to register in the Commons and to include a valid PD/PI Commons ID in the credential field will prevent the successful submission of an electronic application to NIH. See Section III of this FOA for information on registration requirements.
The applicant organization must ensure that the DUNS number it provides on the application is the same number used in the organization’s profile in the eRA Commons and for the System for Award Management. Additional information may be found in the SF424 (R&R) Application Guide.
See more tips for avoiding common errors.
Upon receipt, applications will be evaluated for completeness and compliance with application instructions by the Center for Scientific Review and the participating ICs. Applications that are incomplete or non-compliant will not be reviewed.
Applicants requesting $500,000 or more in direct costs in any year (excluding consortium F&A) must contact a Scientific/ Research Contact at least 6 weeks before submitting the application and follow the Policy on the Acceptance for Review of Unsolicited Applications that Request $500,000 or More in Direct Costs as described in the SF424 (R&R) Application Guide.
Only the review criteria described below will be considered in the review process. Applications submitted to the NIH in support of the NIH mission are evaluated for scientific and technical merit through the NIH peer review system.
For this particular announcement, note the following:
R01 technology development funding announcements are designed to support high risk projects that are not ready for testing biological hypotheses. The objectives should not solve untested biological hypotheses or gain new biological knowledge. Applications should be innovative, include measurable objectives and intermediate milestones, and describe risk management. Risk can be mitigated by preliminary data, theoretical evaluation, alternative approaches, and well described criteria for success and failure. Projects appropriate for a four or five-year R01 should include evidence that the outcome is feasible. The R01 objectives should include functioning prototypes or evaluation of working technology that may not be as efficient, robust, or versatile as the final version, but should demonstrate utility to resolve a significant biomedical problem. The specific aims should include validation of technology against known standards such as synthetic models and characterized, gold-standard biological systems. Projects that are at an intermediate stage, with incomplete preliminary data, but with substantial remaining risk, might be an appropriate for a three-year R01 application with a reduced budget. This strategy minimizes risk by rapidly evaluating project feasibility. Three-year R01 applications minimize risk by rapidly evaluating project feasibility but should have shown strong promise and demonstrated innovation.
Does the project address an important problem or a critical barrier to progress in the field? Is the prior research that serves as the key support for the proposed project rigorous? If the aims of the project are achieved, how will scientific knowledge, technical capability, and/or clinical practice be improved? How will successful completion of the aims change the concepts, methods, technologies, treatments, services, or preventative interventions that drive this field?
For this FOA: Does the proposed technology development have the potential to address a significant unmet need in biomedical research, or open significant new avenues for investigation? Is the potential effect of the technology on biomedical research appropriately broad, or sustained?
Regardless of the inherent risk of the project, assuming that continued development of the technology is successful, would its availability enable new research or significantly facilitate current research?
Is the technology likely to have a practical e ffect on the research community? Does the proposed technology have the potential to be widely adopted by the relevant research community?
Are the PD(s)/PI(s), collaborators, and other researchers well suited to the project? If Early Stage Investigators or those in the early stages of independent careers, do they have appropriate experience and training? If established, have they demonstrated an ongoing record of accomplishments that have advanced their field(s)? If the project is collaborative or multi-PD/PI, do the investigators have complementary and integrated expertise; are their leadership approach, governance and organizational structure appropriate for the project?
For this FOA: Do the investigators have a record of significant technological innovation? Do the investigators demonstrate a willingness to recognize risks and take risks to solve challenging problems?
Does the application challenge and seek to shift current research or clinical practice paradigms by utilizing novel theoretical concepts, approaches or methodologies, instrumentation, or interventions? Are the concepts, approaches or methodologies, instrumentation, or interventions novel to one field of research or novel in a broad sense? Is a refinement, improvement, or new application of theoretical concepts, approaches or methodologies, instrumentation, or interventions proposed?
For this FOA:
Does the research plan test an innovative concept for development of an unproven technology? Is the research plan focused on addressing substantial technical challenges associated with implementing an innovative technology? Is the proposed technology fundamentally new? If it is not new, does it solve a longstanding technical problem in an established technology area? Does the proposed technology effectively address a previously unsolved problem, regardless of whether the approach is novel?
Is the proposal ambitious rather than incremental? Does the proposed project go beyond the current technology development regime in a given area? Will the project take a fundamentally new approach?
Are the overall strategy, methodology, and analyses well-reasoned and appropriate to accomplish the specific aims of the project? Have the investigators included plans to address weaknesses in the rigor of prior research that serves as the key support for the proposed project ? Have the investigators presented strategies to ensure a robust and unbiased approach, as appropriate for the work proposed? Are potential problems, alternative strategies, and benchmarks for success presented? If the project is in the early stages of development, will the strategy establish feasibility and will particularly risky aspects be managed? Have the investigators presented adequate plans to address relevant biological variables, such as sex, for studies in vertebrate animals or human subjects?
If the project involves human subjects and/or NIH-defined clinical research, are the plans to address 1) the protection of human subjects from research risks, and 2) inclusion (or exclusion) of individuals on the basis of sex/gender, race, and ethnicity, as well as the inclusion or exclusion of individuals of all ages (including children and older adults), justified in terms of the scientific goals and research strategy proposed?
For this FOA: Does the project involve an appropriately high level of uncertainty or risk? Is the potential impact commensurate with the level of risk? Would meeting the proposed milestones be sufficient to establish the readiness of the proposed technology for subsequent first attempted application to a biomedical research problem? If feasibility has been established, will the project objectives lead to a working prototype of the technology? If projects are at an intermediate stage with substantial risk remaining to be addressed by feasibility studies, are the reduced scope and duration of the project appropriate for rapidly evaluating feasibility before advancing to future prototype development?
Is the experimental approach reasonable with respect to known issues and concerns of technological feasibility? Are risks clearly addressed and alternative strategies described?
Is the research plan focused on addressing technical challenges rather than proposing hypothesis-driven biomedical research, consistent with stated program goals?
Will completion of the proposed research plan be likely to result in a functioning first embodiment of the technology? Would experimental results from this project be an adequate foundation for the next phase development efforts such as a future R01 project or equivalent? If the project is successful, will the proposed technology be ready for its first application to a biomedical research problem?
Will the scientific environment in which the work will be done contribute to the probability of success? Are the institutional support, equipment and other physical resources available to the investigators adequate for the project proposed? Will the project benefit from unique features of the scientific environment, subject populations, or collaborative arrangements?
For research that involves human subjects but does not involve one of the categories of research that are exempt under 45 CFR Part 46, the committee will evaluate the justification for involvement of human subjects and the proposed protections from research risk relating to their participation according to the following five review criteria: 1) risk to subjects, 2) adequacy of protection against risks, 3) potential benefits to the subjects and others, 4) importance of the knowledge to be gained, and 5) data and safety monitoring for clinical trials.
For research that involves human subjects and meets the criteria for one or more of the categories of research that are exempt under 45 CFR Part 46, the committee will evaluate: 1) the justification for the exemption, 2) human subjects involvement and characteristics, and 3) sources of materials. For additional information on review of the Human Subjects section, please refer to the Guidelines for the Review of Human Subjects.
When the proposed project involves human subjects and/or NIH-defined clinical research, the committee will evaluate the proposed plans for the inclusion (or exclusion) of individuals on the basis of sex/gender, race, and ethnicity, as well as the inclusion (or exclusion) of individuals of all ages (including children and older adults) to determine if it is justified in terms of the scientific goals and research strategy proposed. For additional information on review of the Inclusion section, please refer to the Guidelines for the Review of Inclusion in Clinical Research.
The committee will evaluate the involvement of live vertebrate animals as part of the scientific assessment according to the following criteria: (1) description of proposed procedures involving animals, including species, strains, ages, sex, and total number to be used; (2) justifications for the use of animals versus alternative models and for the appropriateness of the species proposed; (3) interventions to minimize discomfort, distress, pain and injury; and (4) justification for euthanasia method if NOT consistent with the AVMA Guidelines for the Euthanasia of Animals. Reviewers will assess the use of chimpanzees as they would any other application proposing the use of vertebrate animals. For additional information on review of the Vertebrate Animals section, please refer to the Worksheet for Review of the Vertebrate Animal Section.
Reviewers will assess whether materials or procedures proposed are potentially hazardous to research personnel and/or the environment, and if needed, determine whether adequate protection is proposed.
For Resubmissions, the committee will evaluate the application as now presented, taking into consideration the responses to comments from the previous scientific review group and changes made to the project.
For Renewals, the committee will consider the progress made in the last funding period.
For Revisions, the committee will consider the appropriateness of the proposed expansion of the scope of the project. If the Revision application relates to a specific line of investigation presented in the original application that was not recommended for approval by the committee, then the committee will consider whether the responses to comments from the previous scientific review group are adequate and whether substantial changes are clearly evident.
Reviewers will assess the information provided in this section of the application, including 1) the Select Agent(s) to be used in the proposed research, 2) the registration status of all entities where Select Agent(s) will be used, 3) the procedures that will be used to monitor possession use and transfer of Select Agent(s), and 4) plans for appropriate biosafety, biocontainment, and security of the Select Agent(s).
Reviewers will comment on whether the following Resource Sharing Plans, or the rationale for not sharing the following types of resources, are reasonable: (1) Data Sharing Plan; (2) Sharing Model Organisms; and (3) Genomic Data Sharing Plan (GDS).
For projects involving key biological and/or chemical resources, reviewers will comment on the brief plans proposed for identifying and ensuring the validity of those resources.
Reviewers will consider whether the budget and the requested period of support are fully justified and reasonable in relation to the proposed research.
Applications will be evaluated for scientific and technical merit by (an) appropriate Scientific Review Group(s) convened by the Center for Scientific Review , in accordance with NIH peer review policy and procedures, using the stated review criteria. Assignment to a Scientific Review Group will be shown in the eRA Commons.
As part of the scientific peer review, all applications:
Information regarding the disposition of applications is available in the NIH Grants Policy Statement.
A formal notification in the form of a Notice of Award (NoA) will be provided to the applicant organization for successful applications. The NoA signed by the grants management officer is the authorizing document and will be sent via email to the grantee’s business official.
Awardees must comply with any funding restrictions described in Section IV.5. Funding Restrictions. Selection of an application for award is not an authorization to begin performance. Any costs incurred before receipt of the NoA are at the recipient's risk. These costs may be reimbursed only to the extent considered allowable pre-award costs.
Any application awarded in response to this FOA will be subject to terms and conditions found on the Award Conditions and Information for NIH Grants website. This includes any recent legislation and policy applicable to awards that is highlighted on this website.
Recipients of federal financial assistance (FFA) from HHS must administer their programs in compliance with federal civil rights law. This means that recipients of HHS funds must ensure equal access to their programs without regard to a person’s race, color, national origin, disability, age and, in some circumstances, sex and religion. This includes ensuring your programs are accessible to persons with limited English proficiency. HHS recognizes that research projects are often limited in scope for many reasons that are nondiscriminatory, such as the principal investigator’s scientific interest, funding limitations, recruitment requirements, and other considerations. Thus, criteria in research protocols that target or exclude certain populations are warranted where nondiscriminatory justifications establish that such criteria are appropriate with respect to the health or safety of the subjects, the scientific study design, or the purpose of the research.
In accordance with the statutory provisions contained in Section 872 of the Duncan Hunter National Defense Authorization Act of Fiscal Year 2009 (Public Law 110-417), NIH awards will be subject to the Federal Awardee Performance and Integrity Information System (FAPIIS) requirements. FAPIIS requires Federal award making officials to review and consider information about an applicant in the designated integrity and performance system (currently FAPIIS) prior to making an award. An applicant, at its option, may review information in the designated integrity and performance systems accessible through FAPIIS and comment on any information about itself that a Federal agency previously entered and is currently in FAPIIS. The Federal awarding agency will consider any comments by the applicant, in addition to other information in FAPIIS, in making a judgement about the applicant’s integrity, business ethics, and record of performance under Federal awards when completing the review of risk posed by applicants as described in 45 CFR Part 75.205 “Federal awarding agency review of risk posed by applicants.” This provision will apply to all NIH grants and cooperative agreements except fellowships.
For additional guidance regarding how the provisions apply to NIH grant programs, please contact the Scientific/Research Contact that is identified in Section VII under Agency Contacts of this FOA. HHS provides general guidance to recipients of FFA on meeting their legal obligation to take reasonable steps to provide meaningful access to their programs by persons with limited English proficiency. Please see https://www.hhs.gov/civil-rights/for-individuals/special-topics/limited-english-proficiency/index.html. The HHS Office for Civil Rights also provides guidance on complying with civil rights laws enforced by HHS. Please see https://www.hhs.gov/civil-rights/for-individuals/section-1557/index.htmlhttps://www.hhs.gov/civil-rights/for-providers/laws-regulations-guidance/index.html. Recipients of FFA also have specific legal obligations for serving qualified individuals with disabilities. Please see https://www.hhs.gov/civil-rights/for-individuals/disability/index.html. Please contact the HHS Office for Civil Rights for more information about obligations and prohibitions under federal civil rights laws at https://www.hhs.gov/ocr/about-us/contact-us/index.html or call 1-800-368-1019 or TDD 1-800-537-7697. Also note it is an HHS Departmental goal to ensure access to quality, culturally competent care, including long-term services and supports, for vulnerable populations. For further guidance on providing culturally and linguistically appropriate services, recipients should review the National Standards for Culturally and Linguistically Appropriate Services in Health and Health Care at http://minorityhealth.hhs.gov/omh/browse.aspx?lvl=2&lvlid=53.
The Federal Funding Accountability and Transparency Act of 2006 (Transparency Act), includes a requirement for awardees of Federal grants to report information about first-tier subawards and executive compensation under Federal assistance awards issued in FY2011 or later. All awardees of applicable NIH grants and cooperative agreements are required to report to the Federal Subaward Reporting System (FSRS) available at www.fsrs.gov on all subawards over $25,000. See the NIH Grants Policy Statement for additional information on this reporting requirement.
In accordance with the regulatory requirements provided at 45 CFR 75.113 and Appendix XII to 45 CFR Part 75, recipients that have currently active Federal grants, cooperative agreements, and procurement contracts from all Federal awarding agencies with a cumulative total value greater than $10,000,000 for any period of time during the period of performance of a Federal award, must report and maintain the currency of information reported in the System for Award Management (SAM) about civil, criminal, and administrative proceedings in connection with the award or performance of a Federal award that reached final disposition within the most recent five-year period. The recipient must also make semiannual disclosures regarding such proceedings. Proceedings information will be made publicly available in the designated integrity and performance system (currently FAPIIS). This is a statutory requirement under section 872 of Public Law 110-417, as amended (41 U.S.C. 2313). As required by section 3010 of Public Law 111-212, all information posted in the designated integrity and performance system on or after April 15, 2011, except past performance reviews required for Federal procurement contracts, will be publicly available. Full reporting requirements and procedures are found in Appendix XII to 45 CFR Part 75 – Award Term and Conditions for Recipient Integrity and Performance Matters.
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Telephone: 301-402-7469 or 866-504-9552 (Toll Free)
General Grants Information (Questions regarding application instructions, application processes, and NIH grant resources)
Email: GrantsInfo@nih.gov (preferred method of contact)
Grants.gov Customer Support (Questions regarding Grants.gov registration and Workspace)
Contact Center Telephone: 800-518-4726
Fei Wang, Ph.D.
Division of Biophysics, Biomedical Technology and Computational Biosciences
National Institute of General Medical Sciences (NIGMS)
Kadir Aslan, Ph.D.
Division of Pharmacology, Physiology, and Biological Chemistry
National Institute of General Medical Sciences (NIGMS)
D. Craig Hopp, Ph.D.
Division of Extramural Research
National Center for Complementary and Integrative Health (NCCIH)
National Institute of General Medical Sciences (NIGMS)
National Center for Complementary and Integrative Health (NCCIH)
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