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Catalog

GENERAL

Expertise

R&D and project management

Due to our project management system and comprehensive approach, we develop and launch the required product volumes in a short time, reducing costs for our partners. We work according to APQP and PPAP methodologies.

R&D и управление проектами

APQP (Advanced Product Quality Planning)

APQP is a methodology for preparing (including planning and developing) processes to produce a product that meets all customer requirements and expectations. The methodology emphasizes the prevention of potential errors, using tools such as Failure Mode and Effects Analysis (FMEA) and the Control Plan.

The APQP project consists of six phases, each of which includes a set of measures to ensure target quality:

  1. Planning and definition of a management plan;
  2. Product design and development;
  3. Design and process development;
  4. Product and process approval;
  5. Feedback, evaluation, and corrective actions;
  6. Management plan methodology.

PPAP (Production Part Approval Process)

The PPAP process is designed to demonstrate that the supplier has developed its design and manufacturing process to meet customer requirements, minimizing the risk of failure through the effective use of APQP.

PPAP is a series of documents that require formal certification/sign-off by the supplier and approval/sign-off by the customer.

Approval Process for the Production Part

  • Design record with all specifications
  • Authorized Engineering Change Number (AECN)
  • Customer Engineering Approval
  • Defined process
  • Documented process
  • Linkages of process established
  • Process is monitored, analyzed, and improved based on data
  • Records are created, maintained, and retained
  • Validation Test Report
  • Control Plan
  • Process Flow Diagram (PFD)
  • Lab Test Report
  • DFMEA (Design Failure Mode and Effects Analysis)
  • PFMEA (Process Failure Mode and Effects Analysis)
  • MSA Study (Measurement System Analysis)
  • SPC (Statistical Process Control)

PPAP Elements

  • Design records
  • Authorized Engineering Change (note) Documents
  • Engineering Approval
  • DFMEA (Design Failure Mode and Effects Analysis) — Analysis of potential design inconsistencies with a quantitative analysis of the consequences and causes of the inconsistencies
  • Process Flow Diagrams
  • PFMEA (Process Failure Mode and Effects Analysis) — Analysis of potential process inconsistencies with a quantitative analysis of the consequences and causes
  • Control Plan
  • MSA (Measurement System Analysis)
  • Dimensional Results
  • Records of Material Tests
  • Initial Process Studies
  • Qualified Laboratory Documentation
  • Appearance Approval Report
  • Sample Production Parts
  • Master Sample
  • Checking Aids
  • Customer-Specific Requirements
  • Part Submission Warrant (PSW) — This form summarizes the entire PPAP package

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