Quality White Papers & Case Studies
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The Next Leap In Pharma Manufacturing
8/8/2025
Explore how Industry 4.0 integration transforms pharma manufacturing through connected systems, data-driven insights, and predictive, compliant operations.
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The GxP Digital Maturity Model
8/8/2025
Explore how the GMP Digital Maturity Model guides life sciences companies through five stages to improve compliance, efficiency, and profitability with strategic digital adoption.
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The Evolution Of EAM/CMMS In Pharma Manufacturing
8/8/2025
Explore pharma’s shift from paper-based maintenance to modern EAM/CMMS that shows how digital tools boost compliance, reduce downtime, and improve data accuracy and productivity.
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Boston Scientific: Enterprise Asset Management
8/8/2025
Examine how Boston Scientific uses RAM to centralize asset management to boost compliance, efficiency, and visibility for maintenance, calibration, and validation across facilities.
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Biotech Firm Streamlines Maintenance, Calibration & Validation With RAM
8/8/2025
Explore how a U.S. biotech company uses RAM to centralize maintenance, calibration, and validation to improve compliance, efficiency, and visibility across multiple facilities.
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How Bend Bioscience Standardized Operations And Boosted Compliance
8/8/2025
Discover how Bend Bioscience replaced its outdated CMMS with RAM to achieve rapid compliance, boost efficiency across facilities, and cut operational costs by 25%.
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Becton Dickinson: Enhancing Maintenance Compliance
8/8/2025
Learn how BD standardized calibration across 85 sites with a RAM to boost compliance, efficiency, and system integration for scalable, future-ready operations.
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Zero To Final Fill: How HUGEL Implemented Its First Single-Use Lines
8/6/2025
As regulations tighten, biomanufacturers are adopting single-use tech to boost compliance, reduce labor, and streamline fill-finish operations from the ground up.
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Optimizing CHO Cell Culture Using A Design Of Experiments Approach
8/6/2025
Learn how researchers optimized CHO cell culture to boost IgG1 titer to 5.8 g/L and improve viability, which cut development time from 14 days to 12 while enhancing productivity.
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Container Closure Integrity Test Method Development For Autoinjectors
8/6/2025
Discover an autoinjector technology that leverages laser-based headspace analysis for container closure integrity to advance biologic drug delivery with precision, safety, and regulatory confidence.