Asset Management Software Designed Specifically
for Good Manufacturing Practices

Blue Mountain RAM’s integrated functionality was designed from the start for achieving both GMP asset compliance and increased productivity. In Pharmaceutical, Biotech and Medical Device companies multiple layers of coordination are required between your maintenance, facilities, engineering and quality groups. Blue Mountain RAM enables all groups to work together to maintain assets and processes in a validated state.

Blue Mountain RAM enables a quality systems approach for Facilities and Equipment, from equipment selection, installation and qualification to operation, maintenance and calibration. Its maintenance and calibration functionality, combined with powerful workflow, querying and reporting tools, drives the integration required in today’s environment.

Fully Integrated CMMS and EAM Capabilities

Life Sciences companies can no longer afford disparate systems for managing GMP assets. That’s why we chose an integrated approach for Blue Mountain RAM, allowing the complete lifecycle for any type of equipment. Integrated functionality eliminates waste, redundancy and errors, while also reducing the number of applications, IT infrastructure and support costs.

Workflow management is a major driver for compliance and productivity. Blue Mountain RAM’s 3rd generation Workflow Tool is powerful and easy to configure, allowing 21 CFR Part 11 automation that can be set up by your organization.

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