How does Burna AI help CROs and Phase 1 sites?

It lowers the cost to deliver a study, the line a sponsor benchmarks most easily in a bid. Burna AI drafts the CTCAE grade, the per-drug attribution and the safety reports at the encounter, so data management, safety review and adverse event coding arrive largely done, inside the coordinator hours already staffed. Each grade arrives bound to its CTCAE criterion with the source line attached, so the evidence a monitor would query for is already in the record. Every trial is graded to the CTCAE version its protocol names, v5.0 or v6.0, whichever sponsor it belongs to. Coordinators file into Medidata Rave in a signed session the platform verifies by reading the entry back, and the graded record exports for entry into other EDCs. Sponsors see inter-rater agreement per site, so drift between sites shows before the monitoring visit. Quality is what keeps a CRO on the panel afterwards.