AccessBridge helps healthcare teams manage expanded access requests faster, fairly, and with confidence.
❚ The Problem
Expanded access requests are often slowed down by fragmented communication, inconsistent sponsor criteria, manual document preparation, unclear responsibilities, and delayed follow-up. Physicians are short on time, sponsors need to protect patient safety and clinical trial integrity, and IRBs need complete information to review. The result is a high-pressure process that can feel messy, repetitive, and difficult to audit.
❚ The Solution
AccessBridge brings the full request journey into one structured workflow. Physicians can submit patient requests through guided intake, sponsors can review against clear decision criteria, compliance teams can assemble FDA and IRB-ready packets, and all parties can track approvals, logistics, treatment confirmation, and outcomes in one place. The system turns a complex regulated process into a clear, step-by-step case workflow.
❚ Who It’s For
AccessBridge is for physicians, sponsors, IRBs, medical affairs, regulatory teams, and logistics teams involved in expanded access or compassionate use requests. It is especially useful for rare disease, oncology, and specialty biotech settings, where patient needs are urgent, decisions are sensitive, and the process must stay organised, compliant, and accountable.
❚ Key Benefits / Features
AccessBridge includes physician dashboards, guided request forms, sponsor decision criteria, compliance checks, IRB review timelines, document packet generation, logistics tracking, notifications, delegation tools, audit trails, and outcome reporting. It helps reduce missing information, surface blockers early, keep each user focused on their responsibilities, and create a reliable record of what happened, when it happened, and why.
❚ Why It’s Different
AccessBridge is not just a project management dashboard. It is a purpose-built operating layer for expanded access, combining structured clinical intake, sponsor policy logic, compliance readiness, approval history, shipment accountability, and post-use safety outcomes. Instead of simply tracking tasks, it helps each party make better, fairer, and more traceable decisions throughout the life of a patient request.
