November Webinar - Advanced Product Quality Planning (APQP) Process Overview

When:  Nov 19, 2025 from 11:00 AM to 12:00 PM (CT)
Associated with  Audit Division

Join us for our November Webinar - "Advanced Product Quality Planning (APQP) Process Overview" presented by Angelo Scangas.

Session Abstract: 

An ever-growing number of companies must comply with Advanced Product Quality Planning (APQP) requirements. Even those that are not subject to a compliance mandate recognize the APQP process as a product development best practice that improves performance for new product introduction. To implement APQP effectively, companies must account for a series of key considerations that will determine the success of the initiative and ultimately the performance of future product launches.

This presentation provides valuable information and examples for the successful implementation of the APQP process at companies of all sizes and across industries. In addition, this presentation will provide effective techniques for conducting effective audits.

Learning Objectives

  • Discuss the key phases of APQP
  • Integrate compliance requirements with auditing techniques
  • Demonstrate knowledge of APQP and how it relates to the Quality System
  • Describe the importance of APQP to successfully implement the launch of a new product

 

Speaker Bio: 

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Angelo G. Scangas, President

Quality Support Group, Inc., Westford, MA 01960 / 978-430-7611

angelo@qualitysupportgroup.com

 Angelo Scangas is President of Quality Support Group, Inc., an International Consulting and Training organization.

Angelo has a B.S. in Chemical Engineering, M.S. in Manufacturing Engineering and a MBA.  Angelo has more than 30 years of experience in the Medical Device, Automotive, Aerospace, Healthcare and Chemical Industries working in quality systems, product development, manufacturing engineering, quality assurance and process improvement. His background includes product development, risk supplier quality, (ISO 9001, AS9100, ISO 13485, IATF 16949) quality system design and implementation, regulatory compliance and FDA submittals. 

Selecting "yes" to this event does not register you for the event.  This MyASQ event is for informational purposes only.

Please register through the link below:

https://asq.webex.com/weblink/register/redb530ae5ad1adc5e444ca3f64a63a4f

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Instructions on how to attend the Webinar will be provided once registered.
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