Quality records live in spreadsheets and silos.
Control plans sit in one file, results in another, and approvals in email. APQP and PPAP packages are assembled by hand, and measurement studies are kept apart from the parts they relate to. Without one connected system, every audit, traceability request and corrective action starts from scratch, and the same deviation can be found, fixed and repeated without the lesson ever reaching design.
Three steps. Zero guesswork.
Catch drift before it becomes a defect.
Every measurement is charted as it arrives. QMS spots trends inside the limits and flags them while they are still cheap to fix.
From RFQ to manufacturing handover.
Three structured phases organize enquiry, feasibility, planning and product development.
- Enquiry Form
- APQP Matrix
- Team Feasibility
- Quotation
- APQP Time Plan
- Risk Analysis
- Resource Requirements
- Acceptance Note
- MFG Process Design Form
- Tool Buyoff Form
- Part Handover Note
Organize the product approval package.
A structured collection of process planning, verification, submission and change records.
- Process Flow Chart (PFC)
- PFMEA
- Control Plan
- FQP
- Incoming Material Control Plan (IMCP)
- Drawing Evaluation Form
- Material Test
- Part Appearance Approval Form
- Part Submission Warrant (PSW)
- Supplier Details
- Engineering Change Note
Evaluate measurement system consistency.
etavat includes workflows for Variable and Attribute Gauge R&R studies.
Evaluates variation in numerical measurements across appraisers and repeated trials.
Example: shaft diameter measured with a micrometer.
Evaluates consistency when parts are classified into categories such as pass/fail.
Example: multiple inspectors assess the same parts.