The APQR process is often laborious, time-consuming and resource-intensive. However, pharmaceutical companies can meet regulatory requirements while streamlining their processes and driving continuous improvement by adopting innovative approaches like Structured Document Authoring – APQR. Delve deeper into the essence of streamlining APQR processes in this whitepaper: http://go.3ds.com/g4r.
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In the pharmaceutical industry, the demand for aseptic flexible multiformat production lines has increased due to the need for small batches, diverse product portfolios, and compliance with stringent regulatory requirements, including the new Annex 1 of Good Manufacturing Practices (GMP). Learn more by download this sponsored content from Telstar: https://bit.ly/3tuhBYH #ISPE #Annex1 #GMP
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In the pharmaceutical industry, the demand for aseptic flexible multiformat production lines has increased due to the need for small batches, diverse product portfolios, and compliance with stringent regulatory requirements, including the new Annex 1 of Good Manufacturing Practices (GMP). Learn more by download this sponsored content from Telstar: https://bit.ly/3tuhBYH #ISPE #Annex1 #GMP
Automating Format Changes in Pharmaceutical Manufacturing: Enhancing Efficiency, Quality, and ROI
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🟢 Envirotainer invests in new testing chambers to drive innovation Envirotainer, the specialist in temperature-sensitive pharmaceutical shipments, has announced significant enhancements to its testing capabilities, with... Read more on our website today https://lnkd.in/dQUH84Wq Subscribe to our newsletter to stay updated with important industry news https://lnkd.in/dRV4mPk. Follow and use #refindustry for #refrigeration news.
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The pharmaceutical industry is a highly regulated environment, where maintaining compliance and ensuring data integrity are paramount. The ENSUR document management system (DMS) can provide a comprehensive solution to manage and secure sensitive information, streamline workflows, and enhance decision-making. Discover how DocXellent can empower your pharmaceutical company with these transformative benefits here: https://hubs.li/Q0291y5x0 #PharmaCompliance #DocXellentDMS #DataIntegrity
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Read our latest blogpost to find out Top 10 Use Cases of Intelligent Document Processing in the Pharmaceutical Industry. What’s more in the article? Check the slider post below! Read the article here: https://lnkd.in/dNaYFCWa #IntelligentDocumentProcessing #documentprocessing #idp
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In this extract from the NSF white paper on the Quality Management Maturity model, experts explain how they worked with a pharmaceutical company to deploy QMM across global sites. Learn more about this Knowledge Library article here: https://bit.ly/3WdME5v
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Interesting insights through the Case Study on Quality Management Maturity Model when applied across different geographical controls.
In this extract from the NSF white paper on the Quality Management Maturity model, experts explain how they worked with a pharmaceutical company to deploy QMM across global sites. Learn more about this Knowledge Library article here: https://bit.ly/3WdME5v
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The future of pharmaceutical SCM is not just about efficiency and cost-effectiveness but also sustainability. Our blog explores the latest trends: https://lnkd.in/gJ7rjN7s #supplierquality #supplychainmanagement #QMS
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