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Click ‘Get Form’ to open the phs 398 document in the editor.
Begin by filling out the TITLE OF PROJECT section, ensuring it does not exceed 81 characters. This is crucial for clarity.
In the PROGRAM DIRECTOR/PRINCIPAL INVESTIGATOR section, provide your name, degrees, and contact information. Make sure all details are accurate to avoid delays.
For HUMAN SUBJECTS RESEARCH, indicate whether your project involves human subjects and provide necessary assurance numbers if applicable.
Complete the DATES OF PROPOSED PERIOD OF SUPPORT and COSTS REQUESTED sections carefully, as these will impact your funding request.
Review the checklist at the end of the form to ensure all required sections are completed before submission.
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This Policy applies to all research funded or proposed for funding by the Public Health Service of the U.S. Department of Health and Human Services (PHS), including the National Institutes of Health (NIH).
What is the PHS 398 research plan?
The PHS 398 Research Plan form is used only for research, multi-project, and SBIR/STTR applications. This form includes fields to upload several attachments, including the Specific Aims and Research Strategy.
What is the PHS 398 cover page supplement?
The PHS 398 Cover Page Supplement Form is used for all grant applications except fellowships. This form collects information on human subjects, vertebrate animals, program income, human embryonic stem cells, inventions and patents, and changes of investigator/change of institution.
What is the PHS 398 research training program plan?
The PHS 398 Research Training Program Plan Form is used only for Training applications and Multi-project applications with an NRSA Training Component. This form includes fields to upload several attachments including the Program Plan, Faculty Biosketches, and Data Tables.
Mar 16, 2021 Grant Application PHS 398 (Revised 03/2020) Downloadable Instructions and Form Files Notable Changes Made to PHS 398. 03/2021. Form Page 4:
For biological products in BLAs under the PHS Act, FDA has, as a scientific matter, generally not permitted applicants to incorporate information about drug
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