Connect deviations to the evidence behind them
Find recurring deviations and assemble related evidence by product, batch and process step.
Inputs: Authorised batch records, quality events, equipment trends and current procedures.
From observation to completed task
Open a proposed investigation record and track assigned follow-ups through the approved quality workflow.
Prepare a project-document handover from approved quality records
The supporting records include approved specifications, change records and quality procedures.
Qualified staff validate manufacturing and release decisions.
The systems involved
Validated quality-system interfaces, versioned methods and product-specific access controls.
SOS AI configures the local models and tool permissions for this workflow. Actions in business software follow the authority you approve; uncertain cases and actions outside those limits go to the responsible person.
What a useful result must get right
Review detection accuracy and investigation lead time; qualified personnel retain batch-release and medical decisions.