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        Document Management: A Tale of Two Manufacturers 
        Experiences from two TrackWise Digital customers, Arbor Pharmaceuticals and Mikart, Inc., highlight the challenges that companies can face when it comes to document management in the pharmaceutical industry.   Arbor is a virtual pharmaceutical manufacturer with over 40 contract manufacturing organizations (CMOs) and more than 400 change control records per year. The company relies on its...
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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.
      • Blog
        3 Ways the CAPA Process is Like Preparing for the Big Game 
        What do football and corrective and preventive action (CAPA) have in common? More than you may think. As the Philadelphia Eagles and the Kansas City Chiefs prepare for this weekend’s big game, let’s consider how the CAPA process in quality management can be compared to these teams’ game strategy.   In both football and quality...
      • 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.
      • Blog
        Integrated Document Management: Leveraging Technology to Improve Compliance and Efficiency
        Quality is essential for manufacturers in regulated industries, such as Life Sciences, to ensure the safety and efficacy of their products and to comply with industry regulations. However, managing and controlling the large number of documents required to be compliant with these regulations can be a significant challenge.  One solution to this challenge is to...
      • Case Study
        Kadmon Pharmaceuticals chooses TrackWise QMS
        TrackWise allows greater visibility of critical information to employees of all levels, automatically generating reports to management and improving effective decision making, transparency of operational information, and collaboration throughout the organization.
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      • Blog
        Document Management: A Tale of Two Manufacturers 
        Experiences from two TrackWise Digital customers, Arbor Pharmaceuticals and Mikart, Inc., highlight the challenges that companies can face when it comes to document management in the pharmaceutical industry.   Arbor is a virtual pharmaceutical manufacturer with over 40 contract manufacturing organizations (CMOs) and more than 400 change control records per year. The company relies on its...
      • Blog
        3 Ways the CAPA Process is Like Preparing for the Big Game 
        What do football and corrective and preventive action (CAPA) have in common? More than you may think. As the Philadelphia Eagles and the Kansas City Chiefs prepare for this weekend’s big game, let’s consider how the CAPA process in quality management can be compared to these teams’ game strategy.   In both football and quality...
      • Blog
        Integrated Document Management: Leveraging Technology to Improve Compliance and Efficiency
        Quality is essential for manufacturers in regulated industries, such as Life Sciences, to ensure the safety and efficacy of their products and to comply with industry regulations. However, managing and controlling the large number of documents required to be compliant with these regulations can be a significant challenge.  One solution to this challenge is to...
      • 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
        Kadmon Pharmaceuticals chooses TrackWise QMS
        TrackWise allows greater visibility of critical information to employees of all levels, automatically generating reports to management and improving effective decision making, transparency of operational information, and collaboration throughout the organization.
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Root Cause Analysis: Getting to the Root of the Issue… and Getting It Right
Watch this presentation from Sparta, to go below the surface and gain insight into the tools needed to conduct effective RCA.
Capitalizing on the Perfect Storm for Digital Quality Transformation
We discuss how recent events have created the natural catalyst and ideal time for life science organizations to evaluate how they manage quality across their extended enterprise.
HONEYWELL TECHNOLOGY SUMMIT
Honeywell Technology Summit – Creating a Sustainable Future
June 2022- Catch industry expert, Mohit Pateriya (Product Expert @ Sparta Systems) as he shares insights on the future of digital quality, compliance and operational excellence for the life sciences industry at the Honeywell Technology Summit, Manila.
Sparta as QMS partner in IBLC
India Biopharma Leaders Conclave 2022
May 2022- Catch the Sparta team at the 2022 India Biopharma Leaders Conclave in Hyderabad.
Digital Quality Transformation in Action
December 2021 - Join us to learn how your peers are digitally transforming their quality operations and gain insights that improve products, business and patient outcomes while maintaining effective regulatory compliance.
Agenda: Digital Quality Transformation in Action
Tue 14 Dec 2021 As a part of the greater Honeywell family, Sparta Systems combines its 26+ years...
Improving Postmarket Surveillance Across the Life Science Value Network
November 2021 - Join this webinar to learn how to assess your postmarket surveillance program and distributed product tracking systems.
 

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