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ON-DEMAND WEBINAR

Understanding PDA/ANSI Standard 06-2025: A Roadmap for Culture Change

Published Date: August 5, 2025

A robust quality culture is no longer a nice to have—it’s a regulatory and operational imperative. Watch for an in-depth exploration of PDA/ANSI Standard 06-2025: Assessment of Quality Culture, a landmark guidance developed to help life science organizations strengthen and assess their internal quality culture.

This webinar provides a concise overview of the new standard, including its purpose, scope, and structure. You’ll gain actionable insights into why quality culture matters, the critical factors that shape it, and how leadership and organizational enablers drive lasting cultural change. Using real-world scenarios and questions adapted from industry publications, we’ll demonstrate how culture can falter and how this standard offers a practical, proactive tool to assess and improve culture.

Through side-by-side comparisons, you’ll learn how to apply the standard within your own systems and identify areas for improvement using proven models and assessment tools.

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Key Takeaways from the Webinar

  • Understand the core principles and structure of PDA/ANSI 06-2025.
  • Explore key enablers and leadership behaviors that foster a quality-first mindset.
  • Learn to identify cultural breakdowns and implement proactive improvements.
  • Discover real-life examples of quality culture challenges and how this standard can help.
  • Gain tools and frameworks to assess and evolve your organization’s culture with confidence.
Susan Schniepp

Susan Schniepp

Pharmaceuticals Quality Assurance Expert

Susan has over 40 years of quality-assurance experience in the pharmaceutical industry. She has earned several awards from the Parenteral Drug Association (PDA), including Distinguished Author Award, Distinguished Service Award, and Gordon Personeus Award. Serving as a volunteer in a number of capacities, she has served on the PDA Board of Directors from 2011 to...

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Matt Cushing

Vice President, Quality and Science

Matt Cushing is the Vice President of Quality and Science at Nelson Laboratories, where he oversees global initiatives and regulatory interactions for teams across 13 sites to uphold the company’s standards in quality, service, and science. With over 20 years of leadership experience in highly regulated environments, including GMP, GLP, ISO, FDA, and more — Matt brings a deep commitment to quality systems and people-centric leadership. His career at Nelson Labs spans roles from Quality Auditor to Senior Director and now Vice President, during which he has successfully managed global quality integration, high-risk scientific issues, and regulatory responses. Matt is known for building high-performing teams and mentoring future leaders, including facilitating leadership development programs, and participating in DEI and women's mentorship initiatives. A recipient of numerous academic and professional honors, including the President’s Award from the University of Utah and the 2025 Nelson Labs Inspired Mentorship Award — Matt continues to model values-driven leadership with a focus on service, collaboration, and continuous improvement.