• Home
  • Products
    • Quality Management System (QMS) for Regulated Industries
    • Document Management System
    • Design Controls System
    • Risk Management System
    • Change Control System
    • Event Management System
    • Supplier Management System
    • Learning Management System
  • Solutions
    • Medical Device QMS Software
    • Pharmaceutical QMS Software
    • Biotech QMS Software
    • Cannabis & Hemp QMS Software
    • GxP Training
  • Pricing
  • Resources
  • Blog
  • Part 11 LMS
  • Demo
  • Free Trial
  1. Blog
  2. Production Part Approval

Currently browsing "Production Part Approval"

  • QMS

    17 articles

  • QMS

    12 articles

  • 21 CFR Part 11

    9 articles

  • Quality Management Systems

    7 articles

  • Pharmaceutical Manufacturing

    7 articles

  • Quality Management System Software

    7 articles

  • Aviation Industry

    6 articles

  • Compliance Culture

    6 articles

  • cGMP Guidelines

    5 articles

  • Medical Devices

    5 articles

  • ISO 13485

    5 articles

  • FDA Inspections

    4 articles

  • Change Control

    4 articles

  • Laboratory Quality Control

    4 articles

  • CAPA

    4 articles

  • Audit Management

    3 articles

  • Quality Control

    3 articles

  • Clinical Evaluation

    3 articles

  • ISO

    3 articles

  • QA and QC

    3 articles

  • Quality

    3 articles

  • Design Controls

    3 articles

  • Aviation Compliance

    2 articles

  • FDA

    2 articles

  • eQMS Software

    2 articles

  • Operating Management Systems

    2 articles

  • QMSR

    2 articles

  • Digital Transformation

    2 articles

  • DMR

    2 articles

  • ISO 14971

    2 articles

  • Production Part Approval

    Production Part Approval Process (PPAP) in QMS: A Complete Guide

    eLeaP Editorial Team

    September 25, 2025

    7 min read

    Production Part Approval Process (PPAP) in QMS: A Complete Guide

    The Production Part Approval Process (PPAP) is a standardized procedure designed to verify that suppliers can consistently produce parts meeting all customer engineering and quality requirements during actual production. Originally developed by the Automotive Industry Action Group (AIAG), PPAP became the industry benchmark for supplier validation in the automotive supply chain. Due to its effectiveness […]

    Continue reading

About eLeaP

  • About eLeaP®
  • Excellence
  • Quality Management
  • Learning Management
  • Performance Management

Capabilities

  • Quality Management System (QMS)
  • Learning Management System
  • Performance Management System
  • 21 CFR Part 11 LMS
  • 14 CFR Parts 145, 135, 43, 91, 121 LMS
  • Quality Management System Software
  • Quality Management
  • Quality Management Software
  • Quality Management System
  • QMS Software
  • Brochures

Learn

  • eQMS Software
  • QMS
  • Quality System Software
  • Cloud QMS
  • Electronic Quality Management System
  • GMP (Good Manufacturing Practice)
  • FDA Cleared vs Approved:
  • Software as a Medical Device SaMD
  • Pharma Definition: Biotech vs Pharma
  • PMA Meaning
  • cGMP
  • GxP

Help & Tools

  • Resources
  • Glossary
  • eQMS System
  • QMS System
  • Cloud Quality Management System
  • Quality Assurance vs Quality Control
  • ISO 9001:2015
  • ISO 13485 & 21 CFR Part 820
  • ISO 14971
  • 21 CFR Part 11 Compliance
  • Free Downloadable SOPS
  • Sitemap

Get in Touch

(877) 624-7226

support@eleapsoftware.com

  • Contact eLeaP
  • LinkedIn
  • YouTube
  • X
  • Facebook

© 2002 - 2026 Telania, LLC.

  • QMS Privacy Policy