Contact Person

Térésa Nüsse

Tel. +49 2339 9182-214

Production Part Approval Process · Initial Sample Reports

CASQ‑it PPAP creates all reports in compliance with ISO/TS 16949, QS9000, VDA2, Odette, DIN EN 9102, HACCP being required for the production part approval: dimensional report, functional report, material report, capability studies as well as material data sheet and declaration of ingredients with direct link to drawing or recipe. Samplings may be performed by suppliers or customers.


Highlights Production Part Approval Process

  • Standard process initial sample report
  • Automatic report versioning
  • Use of report templates
  • Initial sampling, follow-up sampling 
 and requalification
  • Integrated due-date alert
  • Bi-directional data import / transfer to quality control planning
  • Variable, attributive quality controls, visual inspections, installation tests
  • Import of previous quality control reports’ results
  • Access to CASQ it SPC values measured
  • Measured-value matrix for moulds / cavities for multiple tools
  • Post-sampling approval of the supplier in CASQ it IGI
  • Granting preliminary approvals 
(VDA 2.5)
  • Report form pursuant to VDA / QS9000 / DIN EN 9102
  • Integrated in the CASQ it parts’ life cycle