The greater the detail of work, the more light that is generally needed. Where the general lighting is not adequate for the work being performed, task lighting should be provided at the workstation.
Introduction to Application for Resubmission and Revision applications Who must complete the "Introduction to Application" attachment: An "Introduction to Application" attachment is required only if the type of application is resubmission or revision or if the FOA specifies that one is needed.
An introduction is not allowed for new or renewal applications.
Descriptions of different types of applications are listed here: NIH Types of Applications. Attach this information as a PDF file. See specific instructions on the content of the introduction on the NIH's Resubmission Applications page.
Additional Instructions for Multi-project: The "Introduction" attachment is required for all resubmission and revision applications. The "Introduction" attachment is optional for resubmissions and revisions applications. Although the "Introduction" attachment is optional, you may get a system warning if there is no attachment.
State concisely the goals of the proposed research and summarize the expected outcome sincluding the impact that the results of the proposed research will have on the research field s involved. List succinctly the specific objectives of the research proposed e.
The "Specific Aims" attachment is required. State the specific objectives of the Phase I research and development effort, including the technical questions you will try to answer to determine the Phase I feasibility of the proposed approach and the impact that the results of the proposed research will exert on the research field s involved.
State concisely and realistically what the proposed research is intended to accomplish in terms of its potential for technological innovation and commercial application.
Define the proposed product, process or service to ultimately be developed.
Include milestones for each of the aims as these will be used in the evaluation process. State the specific objectives of the Phase II research and development effort including the impact that the results of the proposed research will exert on the research field s.
Define the proposed product, process, or service to ultimately be developed. Research Strategy Who must complete the "Research Strategy" attachment: The "Research Strategy" attachment is required. Although multiple sections of information are required in the Research Strategy as detailed below, the page limit applies to the entirety of the single "Research Strategy" attachment.
Organize the Research Strategy in the specified order and use the instructions provided below unless otherwise specified in the FOA.
Start each section with the appropriate heading - Significance, Innovation, Approach. That form will capture detailed study information for consolidated human subjects, inclusion enrollment report, and clinical trial information.
Use the Research Strategy section to discuss the overall strategy, methodology, and analyses of your proposed research, but do not duplicate information collected in the PHS Human Subjects and Clinical Trials Information form.
The PHS Human Subjects and Clinical Trials Information form will capture detailed study information, including eligibility criteria; inclusion of women, minorities, and children; protection and monitoring plans; and statistical design and power.
Note for Applicants with Multiple Specific Aims: You may address the Significance, Innovation, and Approach either for each Specific Aim individually or for all of the Specific Aims collectively. Significance Explain the importance of the problem or critical barrier to progress that the proposed project addresses.
Describe the scientific premise for the proposed project, including consideration of the strengths and weaknesses of published research or preliminary data crucial to the support of your application. Additional Instructions for Research: Describe how the concepts, methods, technologies, treatments, services, or preventative interventions that drive this field will be changed if the proposed aims are achieved.
Overall and Other Components: Explain the project's potential to lead to a marketable product, process, or service. Explain how the commercialization plan demonstrates a high probability of commercialization. Innovation Explain how the application challenges and seeks to shift current research or clinical practice paradigms.
Describe any novel theoretical concepts, approaches or methodologies, instrumentation or interventions to be developed or used, and any advantage over existing methodologies, instrumentation, or interventions.
Explain any refinements, improvements, or new applications of theoretical concepts, approaches or methodologies, instrumentation, or interventions.You can use this Availability Plan Template (MS Word 26 pages) to describe how your system will be made available by capturing the hardware and software aspects of your solution setup..
Use this template to: Ensure that your system responds correctly to requests, is adequately maintained and communicates with interfacing components, such as network and servers. The EPA Quality Program provides requirements for conducting quality management activities for all environmental data collection and environmental technology programs performed by or for the Agency.
The primary goal of the program is to ensure that the Agency’s environmental decisions are.
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