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Maximizing the Scientific Value of the NHLBI Biologic Biospecimen Repository: Scientific Opportunities for Exploratory Research (R21)

List of required information for application:

1. Applicant Information: Name, contact information, and affiliation of the principal investigator (PI) and co-investigators, if applicable.

2. Project Title: A concise and descriptive title for the proposed research project.

3. Research Plan: A detailed description of the proposed research project, including the objectives, research design, methods, and expected outcomes.

4. Relevance to NHLBI Mission: A clear explanation of how the proposed research aligns with the mission of the National Heart, Lung, and Blood Institute (NHLBI).

5. Use of Biospecimens: A description of the specific biospecimens from the NHLBI Biologic Specimen Repository that will be utilized in the research and how they will help maximize the scientific value of the stored collections.

6. Significance and Innovation: A discussion of the potential scientific significance and innovation of the proposed research, highlighting any unique aspects or novel approaches.

7. Preliminary Data: Information on any preliminary data or previous work conducted by the PI or co-investigators that supports the feasibility or potential success of the proposed research.

8. Research Team: A brief description of the PI's and co-investigators' qualifications, expertise, and experience relevant to the proposed research.

9. Budget and Justification: A detailed budget plan and justification, including personnel, supplies, equipment, travel, and any other anticipated expenses.

10. Timeline: A proposed timeline for the project, including major milestones and expected completion date.

11. Data Sharing Plan: A description of how the research data, findings, and any derived materials or resources will be shared or made available to the scientific community or other stakeholders.

12. References: A list of references cited in the research plan.

13. Bioethics and Human Subjects: If applicable, a description of any involvement of human subjects and a plan for obtaining informed consent and ensuring ethical compliance.

14. Other Supporting Documents: Any additional documents required by the funding agency, such as letters of support, collaboration agreements, or institutional approvals.

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88%

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93%

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