Deviatta Information

Deviatta handles deviations for pharma manufacturers and CDMOs, from the operator's first account to the CAPA effectiveness review. When something goes wrong on a production floor, the first account is spoken, not written. Deviatta captures it in a voice interview at the end of the shift, on a device the operator already uses, and turns it into a QMS-ready draft with a full audit trail. That is Urd, the first of three modules named for the Norns who weave the threads of what has been, what is, and what must follow. Verdandi carries the investigation: root-cause analysis with the method matched to the event - Is/Is-Not, fishbone (6M), 5 Whys, or link analysis within the batch - with evidence attached and excluded alternatives on the record, plus a recurrence check against the site's deviation history. Skuld carries what must follow: the CAPA plan with named owners and, for actions that warrant it, objective effectiveness criteria and review dates. One incident number runs from capture to the CAPA effectiveness check. Four checkpoints sit along the way, and every one of them is a human approval in your QMS: QA confirms the initiation, accepts the investigation conclusion, closes the deviation with the approved CAPA plan, and closes the CAPA after the effectiveness review. Deviatta closes nothing on its own. AI drafts · humans sign · QA closes, in your QMS. Deviatta is hosted in the EU, and each client's deviation data is stored on the client's own server, in their environment. The workflow is built and demonstrable across all three modules. We are looking for up to three first movers ready to take it into a live manufacturing setting. Learn more at deviatta.com.