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FOR CANCER CENTERS

What does Burna AI do for a cancer center's clinical trials office?

It lowers the cost of every study the cancer center runs, then lets the same research team open more. Burna AI drafts the CTCAE grade, the per-drug attribution and the IRB, sponsor and MedWatch reports inside the coordinator hours already staffed, so each study costs less to deliver. Grading by hand takes 15 to 20 minutes per adverse event when it goes well; with the grade drafted and cited, the coordinator reviews rather than reconstructs, and that time goes to the next study. The technology fee can sit in the study contract, the way a CTMS fee does. Each study is graded to the CTCAE version its protocol names, v5.0 or v6.0. New coordinators practice on synthetic cases before touching real ones, which matters when research staff turnover runs high. Every grade carries its citation, so the evidence a sponsor query asks for is already attached.

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