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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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Strategic Insights on Transforming Quality Management
STRATEGIC INSIGHTS ON TRANSFORMING QUALITY MANAGEMENT
December 2021 - Catch industry experts, from India, as they share insights on the future of digital quality, compliance and operational excellence for the biopharmaceutical industry.
质量4.0: 药企的现代化质量管理之路
September, 2021- 网播会提供如何应用自动化的质量信息管理系统 (QMS) 加速药物公司质量管理的数字化转型。Kobe Yue, Sparta Systems亚太区产品解决方案总监,将在会上与您分享质量管理过程中的主要挑战和国际趋势,以及像质量管理系统 (QMS) 等基础应用的重要性。
Top 5 Business Case Scenarios for QMS Investment
Watch this unique webinar replay as we share industry experiences and insights from our 25 years partnering with Life Science companies on quality management.
 

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