Brain Tumor
American Brain Tumor Association
Type of Organization: Charity
Email Address: grants@abta.org
Funds Available for Clinical Trials:
✗ Research:
✔
Funding Details
Requirements: SUBMISSION OF REQUIRED DOCUMENTS
The ABTA requires the submission of certain financial information, applicant information, regulatory documents, and other documentation (collectively referred to as “Required Policies and Procedures for ABTA Grants and Fellowships Issued November 7, 2023 Page 6 of 27 Documents”). All Required Documents must be submitted and approved by the ABTA prior to the execution of the Grant Agreement. The ABTA reserves the right to request any additional documentation from Grantees prior to or after the execution of a Grant Agreement, renewals, updates, and/or resubmissions of certain Required Documents during the Grant Term (as defined in Section 7). Required Documents include, but are not limited to, the documents described below.
4.1 Financial Information Financial information includes: (a) Taxpayer Identification Number and Certification (for U.S. Grantee Institutions only) via Institutional Form W-9; (b) Certificate of Foreign Status of Beneficial Owner for United States Tax Withholding (for foreign Grantee Institutions only) via Form W-8BEN; and (c) Evidence of Grantee Institution’s Section 501(c)(3) or Section 170(c)(1) tax-exempt status or the international equivalent.
4.2 Applicant Information from each Principal Investigator, Co-Principal Investigator and Lead Mentor (as applicable) Applicant information includes: Photograph for each PI and Co-PI, and NIH formatted biosketch that lists updated funding (current and pending) for each PI, Co-PI and Lead Mentor.
4.3 Regulatory Documents Regulatory documents include: (a) Institutional Review Board (“IRB”) or international equivalent approval for Research Projects involving the use of human subjects (described in Section 3.1); and (b) Institutional Animal Care and Use Committee (“IACUC”) or international equivalent approval for Research Projects involving the use of animals (described in Section 3.4). The above Regulatory Documents must: (a) apply to the same studies proposed in the Research Project; (b) stipulate approval and renewal and/or expiration dates; and (c) be provided in English.
4.4 Other Documentation If the Research Project requires the use of a resource (i.e., drug, biospecimen, animal model and/or data (the “Resource”), that the PI, Co-PI or Grantee Institution does not own or is not publicly available, a letter of support from the owner of the Resource must be submitted on the organization’s letterhead and signed by an authorized signatory. Such authorization letter should confirm the availability of and access to the Resource needed for successful completion of the Research Project.