Quality 4.0: What’s All the Buzz and
Can it Really Impact Our Business?

An FDAnews FREE Webinar • Sponsored by ComplianceQuest
Tuesday, Sept. 22, 2020 • 1:30 p.m. - 2:30 p.m. EDT

With the latest industrial revolution called Industry 4.0, there is also a shift taking place based on the related Quality 4.0 framework. At its core, this new digital transformation is disrupting our current ways of thinking about Quality Processes, Automation, Efficiency Gains, Speed to Market, Data Visibility and Decision based Reporting. To err is human and yet at our fingertips are new technologies that provide the opportunity to greatly reduce the human factor and significantly enhance the ROI for workplace streamlining efforts. So if that’s the case, how do we capitalize on it and what strategic steps and critical toolsets are necessary to being the journey?

In this webinar, we will take a deeper look at the history, evolving processes and platforms and include ways to formulate and apply Quality 4.0 thinking. We will address several key factors including the why, the when and the how decisions companies such as yours will need to build the critical framework to digitally transform your workplace. It’s not complicated and in the end there are only 3 factors that have to be considered: People, Processes and Technology.

From this webinar, you will learn:

  • What is Quality 4.0 and how did it evolve?
  • What are the new functional tools that would enable me and my company to take full advantage of the digital revolution?
  • How is a Quality 4.0 strategic roadmap built and the available tools applied?
  • What does a full implementation of Quality 4.0 look like and how can it impact People, Processes and Technology?
  • What are the key performance metrics (KPIs) needed and how do I begin to calculate and measure?
  • How do I formulate a strategy for digital transformation, communicate it to my superiors and move toward key next steps?

Who Will Benefit

  • Quality Personnel
  • Regulatory Personnel
  • IT Personnel

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Meet Your Presenter


Tim Fischer

Principal Partner, Great Solutions, LLC

Tim Fischer has been in the Life Science compliance arena for 30 years. Beginning his career at Abbott Labs in North Chicago IL in lab operations, manufacturing and technical support, he was able to build on that experience and spent several years as Director of Compliance for 3 different contract manufacturing organizations. He then began working directly with compliance software platforms including Compliance Quest, Pilgrim, ETQ and PrisymID as an Industry SME and now manages a consulting group focused on Quality 4.0 software initiatives, GMP quality systems/auditing and FDA/Supplier remediation.