Pharmaceutical | Blue Mountain

akorn

bausch lomb

Teva

Unither

Leverage GMP-centered functionality

Meet Part 11, Part 58, Part 210, Part 211 and ICH Q8, 9 & 10 compliance. Blue Mountain RAM is designed to be used in compliance with ISO 9000 and the FDA’s GMP & QSR regulations. The software features Part 11 workflow automation, electronic signatures, built-in security controls for pharmaceutical company users, and detailed audit trails.

Blue Mountain Maintenance Management Software

Medicine production in a pharmaceutical industry

Drive productivity and lean manufacturing

Meter-based or time-based scheduling, paperless SOPs, and measurement data templates streamlines work and reduces scrap and errors. Simplify the creation of events for both schedule-based planned work and on-demand corrective work with Blue Mountain RAM’s robust workflow automation.

Extend equipment lifecycles

Harmonize pharmaceutical equipment maintenance and calibration, spare parts management, scheduling, and work execution functionality to extend equipment lifecycles and drive lower production costs. Electronic records in Blue Mountain RAM track pertinent data of GMP equipment and provide visibility into asset performance from induction to retirement.

Everything you need to bring safe & effective therapies to market

Blue Mountain RAM gives you the necessary tools for mastering maintenance and calibration management of GMP equipment.

Electronic Records

Centrally track critical asset information such as asset information, work performed, and equipment status in a GMP environment.

Part 11 Workflow Automation

Automatically route work requests for approval, generate new work orders, and notify technicians of upcoming work, while complying with 21 CFR Part 11.

Robust Audit Trails

Permanently capture old and new values, audit reason, date and time, and the name of the user making changes.

Electronic Work Plans

Provide technicians necessary SOPs with detailed step-by-step tasks and the ability to record acceptance criteria to ensure productivity and compliance.

Add Similar and Asset Enrollment

Built-in functionality streamlines the addition of new equipment and instruments into the system.

Storeroom Management

Storeroom functionality manages spare parts, re-order parts, and tracks like-for-like parts.

Measurement Data

Sophisticated measurement data collection capabilities saves technicians time and ensures accuracy.

Out Of Tolerance

Automatically trigger Out of Tolerance notifications when they arise – ensuring the results are not overlooked.

Standards Management

Automatically provide a warning or lock down standards that are out of calibration or overdue for calibration.

On demand business intelligence

Blue Mountain RAM features robust, on demand business intelligence. Gain in-depth visibility into pharmaceutical assets, manufacturing processes, and all facilities across the enterprise. Improve control of compliance across organizations and get the greatest return on investment.

Productivity-focused interface

Blue Mountain RAM's productivity-focused interface is easy to use and enables fast adoption for new users. A responsive design for any screen size enables quick access to records and pertinent information. The software drives productivity by providing tools to streamline work execution.

Achieve GMP compliance and maximize profitability with Blue Mountain.

Our industry-leading software was designed for the Life Sciences. We're here to help you manage the complete lifecycle of your assets and put best practices in place.

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Asset Management Software for Pharmaceutical