Could Veeva or Medidata add AI adverse event grading as a feature?

EDC and safety systems such as Veeva and Medidata sit downstream of the attribution decision: they record what the investigator decided. Burna AI works upstream, where the investigator is making that decision. It grades each adverse event on CTCAE, scores attribution against every drug in the regimen with WHO-UMC and Kramer, and shows the line in the medical record and the reasoning behind each result before the investigator signs. That is an architecture rather than a form field: twelve specialized agents in a cascading constraint pipeline, with two patents filed. Burna AI works alongside the downstream systems, and a coordinator can file the signed adverse event log and SAE form into Medidata Rave.