FEATURED ARTICLES

• 3 Reasons Why Manufacturers And CDMOs Are Integrating QA, QC, And Manufacturing

  Life sciences manufacturers are integrating QA, QC, and production to boost efficiency, reduce downtime, and scale smartly. Discover how Industry 4.0 technologies are reshaping operations.

• Navigating Digital Transformation For Pharmaceutical CDMOs

  Discover how CDMOs can modernize operations, safeguard data integrity, and improve audit readiness with practical strategies for connecting systems and reducing validation burdens.

• Calculating The ROI Of EAM/CMMS For Pharma Manufacturers And CDMOs

  Learn how modern EAM and CMMS systems help pharma manufacturers reduce risk, improve compliance, and cut costs, as well as nine signs it’s time to move beyond outdated asset management practices.

• A Guide To EAM/CMMS Selection For Contract Manufacturers

  CDMOs face rising complexity in multi-client operations. Learn how modern EAM and CMMS systems enable agility, compliance, and scalability to transform asset management into a strategic advantage.

• The Roadmap To Asset Performance Management In Life Sciences

  Find out how asset performance management boosts reliability, compliance, and efficiency in life sciences, which guides organizations from reactive fixes to predictive optimization.

• Exploring The Potential Of Agentic AI

  Discover how agentic AI is poised to transform Enterprise Asset Management in regulated industries to enhance compliance, reduce downtime, and bridge fragmented systems for resilient operations.

• A Guide To CMMS/EAM Readiness In Pharma Manufacturing

  Discover why pharmaceutical manufacturers should adopt CMMS/EAM systems to show how they boost equipment reliability, ensure compliance, control costs, and improve decision-making.

• GMP Calibration Management

  Learn why generic EAM systems fall short in regulated industries and how purpose-built solutions ensure compliance, efficiency, and audit readiness.

• The Next Leap In Pharma Manufacturing

  Explore how Industry 4.0 integration transforms pharma manufacturing through connected systems, data-driven insights, and predictive, compliant operations.

• The GxP Digital Maturity Model

  Explore how the GMP Digital Maturity Model guides life sciences companies through five stages to improve compliance, efficiency, and profitability with strategic digital adoption.

• The Evolution Of EAM/CMMS In Pharma Manufacturing

  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.

• Enterprise Asset Management (EAM) For Life Sciences

  Discover a guide that helps regulated organizations choose and implement systems to boost compliance, efficiency, and asset reliability across operations.

• Boston Scientific: Enterprise Asset Management

  Examine how Boston Scientific uses RAM to centralize asset management to boost compliance, efficiency, and visibility for maintenance, calibration, and validation across facilities.

• Biotech Firm Streamlines Maintenance, Calibration & Validation With RAM

  Explore how a U.S. biotech company uses RAM to centralize maintenance, calibration, and validation to improve compliance, efficiency, and visibility across multiple facilities.

• How Bend Bioscience Standardized Operations And Boosted Compliance

  Discover how Bend Bioscience replaced its outdated CMMS with RAM to achieve rapid compliance, boost efficiency across facilities, and cut operational costs by 25%.

• Becton Dickinson: Enhancing Maintenance Compliance

  Learn how BD standardized calibration across 85 sites with a RAM to boost compliance, efficiency, and system integration for scalable, future-ready operations.