ResolQa turns defects, CAPA, supplier issues, audits, and complaints into one controlled route from signal to proof.
When a defect starts in a spreadsheet, a supplier replies by email, and evidence is rebuilt before an audit, the route disappears. ResolQa turns every loose signal into one accountable quality story.
Controlled route
ResolQa is structured around the route quality teams already need: record the event, coordinate the work, and prove the outcome when auditors or customers ask.
Defects, complaints, supplier issues, and audit findings enter a consistent intake path with severity, source, part, line, and owner context.
Owners, containment, investigation, approvals, supplier replies, and effectiveness checks stay connected instead of splitting across messages.
Every decision, response, approval, and attachment becomes a review-ready trail for customers, management reviews, and auditors.
The controlled route carries each issue from intake to ownership, linked CAPA, verification, and evidence without rebuilding the story later.
Scroll or select a module to see how the same quality route adapts to the work your team handles every day.
Record nonconformances, assign owners, classify severity, and connect each event to evidence before it becomes a repeat issue.
Keep investigation, corrective actions, approvals, and effectiveness checks in one workflow that is easy to review.
Issue SCARs, request evidence, compare supplier trends, and follow repeat defects back to source.
Turn findings into actions and keep the evidence trail connected to each issue, supplier, and closure decision.
Link customer issues to defects, supplier events, CAPA, and closure communication without losing the thread.
Photos, severity, part number, line, and containment owner start in one record.
Investigation stays tied to corrective action, approval, and verification.
SCAR response, due date, and evidence are tracked without inbox hunting.
Actions, approvals, attachments, and closure proof are export-ready.
Complaint response links to investigation, action, and final proof.
See defects, CAPA, audits, supplier responses, and repeat issues in one accountable operating rhythm.
View workflow
Understand containment status, overdue actions, and production risk without waiting for a weekly spreadsheet.
View workflow
Issue SCARs, collect evidence, compare suppliers, and show whether corrective action actually worked.
View workflowResolQa keeps the system close to the way teams operate: inspection, production line, supplier response, and management review stay connected through one route.
Common quality routes across defects, CAPA, supplier response, and audit proof.
A coating issue appears across two lines. ResolQa links it to prior NCRs, starts containment, and flags the supplier pattern.
Root cause, corrective action, owner, approval, and effectiveness check stay visible in one timeline.
The team exports the complete trail instead of rebuilding evidence from inboxes and spreadsheets.
Annual SaaS pricing for U.S. manufacturing teams. Start with one plant, then add suppliers, sites, and validation support as your quality system matures.
Billed annually. For one facility moving defects and CAPA out of spreadsheets.
Book walkthroughBilled annually. For quality teams managing suppliers, complaints, and audits in one route.
Book walkthroughFor multi-site manufacturers with regulated workflows, supplier networks, or enterprise controls.
Contact salesImplementation starts from €2,900 depending on migrated workflows, supplier setup, and validation scope.
No. ISO-driven teams are a natural fit, but the platform is designed around closed-loop quality work: defects, CAPA, supplier quality, audits, complaints, and evidence.
The intended adoption path is practical: start with one workflow, migrate active records, and use reporting exports to reduce spreadsheet dependency over time.
The supplier workflow is designed for controlled response collection, evidence requests, due dates, and SCAR status without forcing every supplier into the same internal workspace.
ResolQa is positioned around resolution speed and evidence clarity for manufacturing teams, with Defects, CAPA, and Supplier Quality as the first-class workflows.
We will tailor the walkthrough around defects, CAPA, supplier quality, audits, or complaints.