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Global Brain and Nervous System Disorders Research Across the Lifespan (R01 Clinical Trials Optional)

List of required information for application:

1. Project Title: The title of the proposed research project.

2. Project Summary: A brief summary describing the objectives, significance, methods, and expected outcomes of the project.

3. Research Plan: A detailed description of the research plan, including the specific aims, background, hypothesis, research design, data collection and analysis methods, and timeline.

4. Collaboration Details: Information about the collaborative nature of the project, including the names and affiliations of all collaborating scientists from U.S., LMIC, and UMIC institutions.

5. Budget: A detailed budget breakdown of the funds requested for the project, including personnel salaries, research supplies, equipment, travel expenses, and any other relevant costs.

6. Justification: A justification explaining why the proposed research is important and how it addresses the specific objectives of the funding opportunity.

7. Qualifications: Information about the qualifications and expertise of the principal investigator and all key personnel involved in the project.

8. Institutional Support: Documentation of support from the applicant institution and any collaborating institutions, including letters of support or commitment.

9. Ethical Considerations: A description of any ethical considerations or potential risks associated with the research, including plans for informed consent, protection of human subjects, and animal welfare.

10. Data Sharing: A plan for data sharing and dissemination of research findings, including any potential limitations or restrictions on data sharing.

11. Prior and Current Funding: Information about any prior or current funding received for the proposed research project, including the funding source, grant title, and duration.

12. Freedom of Information Act (FOIA) Waiver: If applicable, a request for a waiver of the FOIA requirements to protect confidential or proprietary information.

13. Compliance: Assurance of compliance with all relevant regulations, policies, and guidelines, including human subjects protection, animal welfare, biosafety, and responsible conduct of research.

14. References: A list of references cited in the research plan and any supporting documents.

15. Supporting Documents: Any additional supporting documents required by the funding organization, such as a biosketch, letters of collaboration, or additional project-specific materials.

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Eligible Applicants

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Eligible Activities

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88%

Approval rating across all Canadian funding programs

93%

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