NEWSROOM

Category: Calibration

Asset performance in GMP manufacturing is a compliance issue, not just an efficiency metric. Learn five practical ways to reduce downtime, prevent deviations, and bring critical assets under control—without a massive digital overhaul.
Most RFPs say “must be 21 CFR Part 11 compliant,” but that phrase is meaningless without specifics. This checklist gives you testable demo criteria for Part 11 controls, audit trails, validation support, cybersecurity, mobile/offline workflows, and integration traceability—so you can score vendors on evidence, not marketing claims.
Purpose-built life sciences EAM/CMMS platforms don’t just manage work orders — they reduce the compliance workload that comes with validation, upgrades, and audit readiness. Here’s what “purpose-built” really means for Part 11 controls, maintenance and calibration, and time-to-value.
Predictive signals are reshaping GMP maintenance. These seven metrics—PM compliance, OOT velocity, MTBF trends, and more—help you spot risks months before audits and show clear progress toward quality maturity. Learn how to track, interpret, and act
Compare validation burden, OOT workflows, and TCO. Why SAP PM customization extends 6-18 months vs. 8-12 weeks for purpose-built calibration systems.
Seamlessly connect enterprise and operational data. Discover how Blue Mountain’s RAM Connect integrates SAP ERP with RAM—eliminating duplicate entry, maintaining validated audit trails, and giving life sciences manufacturers real-time visibility across maintenance, calibration, and business systems.

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