Blue Mountain Cell & Gene Tech Expo August 2025: GMP And Regulatory Compliance
As organizations in pharmaceuticals, cell and gene therapy, biotech, medical devices, and contract manufacturing scale operations and expand across facilities, they face mounting challenges in maintaining compliance, efficiency, and asset performance within increasingly complex regulatory environments. In this video, Keith Kyle, Executive Director at Blue Mountain, explores the evolving EAM needs of GMP-regulated industries and how Blue Mountain RAM is uniquely designed to meet them. Discover how RAM’s purpose-built, all-in-one EAM, CMMS, and APM platform delivers pre-validated, configurable workflows, advanced analytics, and integrated maintenance and calibration management.
Learn from real-world use cases, see how RAM Connect enables real-time IT/OT integration, and find out how your organization can shift from reactive to optimized asset performance strategies.
Get unlimited access to:
Enter your credentials below to log in. Not yet a member of Cell & Gene? Subscribe today.