Conflict of Interest

Statutes & Regulations

U.S. Public Health Service Regulations

Promoting Objectivity in Research (42 CFR Part 50 Subpart F)

This is incorporated into all PHS proposals and awards. In addition, many private foundations have adopted the PHS regulation.

Public Health Service Agencies

Public Access Information for PHS-Funded Projects 

Within five days of a written request, ±«Óãtv will make information available to the public concerning any Significant Financial Interest (SFI) disclosed to the university that meets the following three criteria:

  1. The SFI was disclosed and is still held by the Senior/key personnel as defined in the PHS regulation;
  2. The university has determined that the SFI is related to the PHS-funded research; and
  3. The university has determined that the SFI is a Financial Conflict of Interest (FCOI).

Pursuant to federal regulations and ±«Óãtv policy, the information that the ±«Óãtv Conflict of Interest Program Manager will make available to any requestor shall include, at a minimum, the following:

  1. The Investigator's name;
  2. The Investigator's title and role with respect to the ±«Óãtv research project;
  3. The name of the entity in which the SFI is held;
  4. The nature of the SFI;
  5. The approximate dollar value of the SFI (dollar ranges are permissible), or a statement that the interest is one whose value cannot readily be determined through reference to public prices or other reasonable measures of fair market value.

To submit a request, please send an e-mail to coi-research@usf.edu.

If e-mail is not available, please send a written letter of request to the following address:
COI Program Manager
±«Óãtv Research & Innovation
Research Integrity & Compliance
ATTN: Public Accessibility Request
3702 Spectrum Boulevard, Suite 155
Tampa, FL 33612

NSF Grantee Standards

In its rds, the NSF has three separate sets of conflict of interest standards related to the financial and program management of federal grants, each governing a different area:

  • Financial management
  • Property management
  • Procurement management. 
FDA Financial Disclosure Regulation

The requires an applicant whose submission relies in part on clinical data to disclose certain financial arrangements between sponsor(s) of the covered studies and the clinical investigators and certain interests of the clinical investigators in the product under study or in the sponsor of the covered studies. A potential source of bias in clinical studies is a financial interest of the clinical investigator in the outcome of the study due to the:

  • way payment is arranged (e.g., a royalty)
  • investigator having a proprietary interest in the product (e.g., a patent)
  • investigator having an equity interest in the sponsor of the covered study