I already own an APQP software package which generates a Design FMEA (DFMEA), Design Verification Plan & Report (DVP&R), Process FMEA (PFMEA) and Control Plan for my products and processes. Why should I consider Quality Plus™?
My APQP Software has several links between the Process FMEA (PFMEA) and Control Plan. How do I know if the links are correct?
You claim that Quality Plus™ is faster than competing APQP software packages in generating APQP documents like the Design FMEA (DFMEA), Process FMEA (PFMEA) and Control Plan and that its documents are easier to maintain. How can this be?
I only create a Design FMEA (DFMEA) and Design Verification Plan & Report (DVP&R) for my products. Can I still use the Quality Plus™ Software and the Quality Plus Structured Design and Process Improvement Methodology?
I only create a Process FMEA (PFMEA) and Control Plan for my products and processes. Can I still use the Quality Plus™ Software and the Quality Plus Structured Design and Process Improvement Methodology?
Can Quality Plus™ and the Quality Plus Structured Design and Process Improvement Methodology help me with my Six Sigma efforts?
