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Human Research Protection Program Independent Review Board Software

Overview


Software, Web & Mobile Development
Athens, Georgia, United StatesPosted: August 29, 2026Deadline: September 15, 2026

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SUMMARY


The organization is seeking software to manage the full lifecycle of human subject research protocols and independent review board activities. The solution must provide configurable workflows, compliance-focused audit trails, collaboration tools, meeting management, dashboards, and customizable reporting.

KEY REQUIREMENTS


CONTRACT DURATION


60 months

TIMELINE


Sourcing Event Published: August 27th, 2026

Sourcing Event Closing: September 15th, 2026

Proposal Evaluation Completed: September 29th, 2026

Negotiations Invitation Issued: October 13th, 2026

Negotiations with Identified Suppliers: October 27th, 2026

Final Evaluation: November 17th, 2026

Finalize Contract Terms: December 8th, 2026

Notice of Intent to Award: December 15th, 2026

QUESTION DEADLINE


September 13, 2026

CONTACTS


Primary procurement contact — name, title, email, and phone

Additional decision-makers and their departments

Issuing Agency


University Of Georgia

Organization overview and procurement intelligence available on paid plans.
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DESCRIPTION


The organization seeks a comprehensive Human Research Protection Program Independent Review Board software solution to modernize the management, oversight, and compliance of human subject research. The platform should support the complete research protocol lifecycle, including submission, review, modification, renewal, approval, monitoring, reporting, and closure.

The solution must provide configurable workflows with automated routing, notifications, and approvals; electronic document management with version control and auditability; multi-user collaboration; and real-time updates. It should capture searchable, detailed audit metadata, including user IDs, timestamps, prior and new values, and contextual information. Authorized users must be able to manually edit workflow states and update workflows as regulations change without vendor involvement.

Additional capabilities should include dynamic data-entry fields, integration with internal and external data sources, meeting scheduling, agenda creation, attendance tracking, minute documentation, role-based real-time dashboards, and robust reporting with customizable queries and visualizations.

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Frequently asked questions


When is the submission deadline?
This RFP closed on September 15, 2026 and is no longer accepting submissions.
Who issued this RFP?
It was issued by University Of Georgia. The work is located in Athens, Georgia, United States.
Who is a good fit for this opportunity?
  • Healthcare compliance and research administration software provider
  • Experience delivering IRB, human research protection, or clinical research management platforms
  • Strong capabilities in workflow automation, electronic document management, and audit trails
  • Proven expertise with configurable reporting, dashboards, and data integrations
  • Experience supporting regulatory environments and evolving compliance requirements

Analysis generated by Settle AI from the source RFP.

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