Secure your spot now before time runs out. Learn about regulatory requirements for computerized systems in the pharmaceutical, biotech, or medical device industry and explore tried, tested, and internationally recognized methods of meeting those requirements. GAMP guidance provides a pragmatic and effective framework for achieving computerized systems that are fit for intended use and meet current regulatory requirements, by building upon existing industry good practice in an efficient and effective manner. Learn More: https://hubs.la/Q02q1r-j0 #ISPE #gamp #ispetraining
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Secure your spot now before time runs out. Learn about regulatory requirements for computerized systems in the pharmaceutical, biotech, or medical device industry and explore tried, tested, and internationally recognized methods of meeting those requirements. GAMP guidance provides a pragmatic and effective framework for achieving computerized systems that are fit for intended use and meet current regulatory requirements, by building upon existing industry good practice in an efficient and effective manner. Learn More: https://hubs.la/Q02r8C6w0 #ISPE #gamp #ispetraining
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Learn about regulatory requirements for computerized systems in the pharmaceutical, biotech, or medical device industry and explore tried, tested, and internationally recognized methods of meeting those requirements. GAMP guidance provides a pragmatic and effective framework for achieving computerized systems that are fit for intended use and meet current regulatory requirements, by building upon existing industry good practice in an efficient and effective manner. Learn More: https://hubs.la/Q02mLyGF0 #ISPE #gamp #ispetraining
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Learn about regulatory requirements for computerized systems in the pharmaceutical, biotech, or medical device industry and explore tried, tested, and internationally recognized methods of meeting those requirements. GAMP guidance provides a pragmatic and effective framework for achieving computerized systems that are fit for intended use and meet current regulatory requirements, by building upon existing industry good practice in an efficient and effective manner. Learn More: https://hubs.la/Q02lDlD90 #ISPE #gamp #ispetraining
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Learn about regulatory requirements for computerized systems in the pharmaceutical, biotech, or medical device industry and explore tried, tested, and internationally recognized methods of meeting those requirements. GAMP guidance provides a pragmatic and effective framework for achieving computerized systems that are fit for intended use and meet current regulatory requirements, by building upon existing industry good practice in an efficient and effective manner. Learn More: https://hubs.la/Q02pByY40 #ISPE #gamp #ispetraining
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Explore the significant costs associated with failed drug and device launches, and the impact on pharmaceutical companies, in our upcoming webinar with @FiercePharma on April 9, 10am ET. Learn how to navigate challenges from early R&D through to commercialization, avoiding common pitfalls and maximizing the potential for success. Register here to attend the webinar or access the recording, here: https://lnkd.in/diQ934Zd #regulatory #clinicaltrials #drugdiscovery
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As many know, maintaining high standards in the pharmaceutical industry is critical. A recent article in Control Design by Anna Townshend explores the impact of automated inspection systems on pharmaceutical manufacturing standards and how they enhance accuracy and ensure compliance with stringent regulations. These systems significantly reduce human error, streamline production processes, and help us stay ahead of evolving standards. It's a compelling read, and Darryl Peterson offers valuable insights for anyone involved in pharmaceutical manufacturing. Read More at https://bit.ly/4bFf9j0 #PharmaceuticalEngineering #Automation #VisionSystems #QualityControl #IndustryStandards
Meeting Pharmaceutical Manufacturing Standards With Automated Inspection
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As many know, maintaining high standards in the pharmaceutical industry is critical. A recent article in Control Design by Anna Townshend explores the impact of automated inspection systems on pharmaceutical manufacturing standards and how they enhance accuracy and ensure compliance with stringent regulations. These systems significantly reduce human error, streamline production processes, and help us stay ahead of evolving standards. It's a compelling read, and Darryl Peterson of Antares Vision Group | Life Science offers valuable insights for anyone involved in pharmaceutical manufacturing. Read More at https://bit.ly/4bFf9j0 #PharmaceuticalEngineering #Automation #VisionSystems #QualityControl #IndustryStandards
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Join us for an insightful episode of the Codebeamer Decoded series on how #ALM can accelerate your #digitaltransformation journey! Discover the latest industry standards and regulations in #MedTech, and learn how our solutions can help you meet requirements. Hear how leading #MedicalDevice and Pharmaceutical companies are using ALM to drive innovation, ensure compliance, and deliver high-quality products faster. https://lnkd.in/e7Vibpqq
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The benefits of implementing continuous manufacturing-from greater quality and reduced operational expenses to shrinking time to market- are well understood by industry. Nevertheless, widespread adoption of this technology in the pharmaceutical industry is slow due to potential financial. Visit us at #ifpac2024 today or contact Richard Steiner to learn how #pharmatechassociates can help you achieve the benefit of pharmaceutical continuous manufacturing. #usp #continuousmanufacturing
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An effective validation solution is essential to confirm the success or failure of the process, whether in pharmaceutical manufacturing, healthcare facilities, research centres or other life science organisations. Find out more and discover why bio-decontamination services provide more than just validation 👇 https://lnkd.in/eKBEpCNj #Protak #biodecontamination #validation
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