Provide high level expert consultation to the University of Minnesota (UMN) to facilitate compliance with Food and Drug Administration (FDA) research.Respondents are prohibited from contacting the identified department about this RFP while in process.Before submitting questions about the RFP via the Questions Tab, read and review the Supplier Process and Information Attachment and ALL Attributes in the Attributes Tab, especially Background and Project Summary/Scope of Work. These provide valuable information and address frequently asked questions.Remember to submit your response, including attachments, early to allow time to correct errors. The submission deadline is a hard close. The system will reject responses with errors and will NOT allow late submissions.