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        2023 Honeywell Users Group
        This three-day event invites Honeywell customers from around the world to learn how businesses handle challenges in fast-paced industries.
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        Root Cause Essentials: Using the PDCA Approach to Support Continuous Improvement
        Studies show that continuous improvement increases productivity, profit, and customer satisfaction and creates less waste. In this blog post, Sparta's Zillery Fortner shows us how the PDCA cycle supports continuous improvement.
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        Quality Systems in the Digital Era: Are You Ready for the Future?
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        Finalized: EU Publishes GMP Annex 1 Revision
        The EU has published its long-anticipated revised GMP Annex 1 for the manufacturing of sterile drug products.
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        Harmonizing Quality and Manufacturing Excellence through Digitization and to Support Pharma 4.0
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        Eisai’s TrackWise Digital Conversion: From On-Premises to the Cloud
        The company continues to automate key quality processes since conversion to TrackWise Digital.
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    • FEATURED CONTENT
      • Event
        2023 Honeywell Users Group
        This three-day event invites Honeywell customers from around the world to learn how businesses handle challenges in fast-paced industries.
      • Event, Webinar
        Quality Systems in the Digital Era: Are You Ready for the Future?
      • Event, Webinar
        Harmonizing Quality and Manufacturing Excellence through Digitization and to Support Pharma 4.0
      • Blog
        Root Cause Essentials: Using the PDCA Approach to Support Continuous Improvement
        Studies show that continuous improvement increases productivity, profit, and customer satisfaction and creates less waste. In this blog post, Sparta's Zillery Fortner shows us how the PDCA cycle supports continuous improvement.
      • Blog
        Finalized: EU Publishes GMP Annex 1 Revision
        The EU has published its long-anticipated revised GMP Annex 1 for the manufacturing of sterile drug products.
      • Case Study
        Eisai’s TrackWise Digital Conversion: From On-Premises to the Cloud
        The company continues to automate key quality processes since conversion to TrackWise Digital.
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How to successfully transition to a cloud QMS
Life sciences companies are used to having tight control over their computer systems, upgrade schedules and validation cycles....
Where are you on the quality management maturity spectrum?
Life sciences manufacturers have diverse quality management capabilities - from emerging companies that are still struggling with foundational...
Three reasons to take your Document Management digital
How does your organization manage important documents like policies and specifications? If you thought of a person or...
All Aboard: How to build a culture of quality, not just compliance
In a proprietary study issued by Sparta Systems in 2019, 66 percent of life sciences professionals said compliance...
Quality vs. Compliance: What is the difference and what are the common pitfalls?
As a life sciences manufacturer, compliance with industry regulations is a top priority for your quality management team....
7 Must-Have Quality KPIs
Thank you to all who took interest in our ‘7 Must-Have Quality KPIs’ webinar with our partner, Process...
QMS software validation best practices
Over the last two decades, the lack of clarity around FDA computer system validation (CSV) has created several...
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