CMMS for the pharmaceutical sector: quality and regulatory compliance
Move away from spreadsheets and binders. Gain flawless traceability and meet the quality and regulatory requirements of the pharmaceutical industry with our AQ Manager CMMS.
Why choose our CMMS for the pharmaceutical sector?
Operational mastery at the service of quality.
Reduction of non-compliance risk
Controlled maintenance ensures that equipment remains in a qualified and validated state. Every documented action contributes to GMP compliance, secures product conformity, and limits quality deviations, non-compliant batches, or recalls.
Production equipment availability
Preventive planning and critical equipment management reduce unplanned downtime on sensitive lines. Your production maintains continuity and your delivered volumes gain reliability.
Optimization of productivity and costs
The CMMS maximizes machine availability and limits costly production shutdowns, quality deviations, and raw material losses. It saves teams time and reduces emergency costs.
Strengthening traceability and audit readiness
The CMMS centralizes the history of interventions, controls, and equipment data with full traceability and data integrity (ALCOA+). It facilitates audits and provides the expected evidence (GMP, Annex 11, 21 CFR Part 11).
Tailor-made features for the pharmaceutical industry
Preventive maintenance management
Define, plan, and track preventive maintenance operations based on calendar deadlines, counters, or usage conditions. Interventions are automatically triggered and recorded in the system.
Asset and stock management
Centralize equipment data (files, characteristics, history, documentation, etc.) and ensure the tracking of spare parts, consumables, and stock levels. Stock movements and assignments to interventions are automatically tracked.
Intervention and resource planning
Organize maintenance interventions, assign resources, and manage technician schedules. Operations can be prioritized based on equipment criticality and production constraints.
Automatic report generation
Automatically produce intervention reports and activity summaries. Technical, regulatory, and quality documentation is centralized and associated with equipment and interventions.
Discover all the features of our CMMS to optimize your maintenance
Would you like to learn more about the CMMS dedicated to the pharmaceutical industry?
Maintenance software for all companies in the sector
Pharmaceutical laboratories
Production and packaging sites subject to regulations, with strict control of machines, methods, and quality documents.
Contract manufacturers
Companies producing for multiple contracting parties, with multi-product environments requiring total traceability, high reactivity, and precise intervention planning.
Biotech
Innovative players with sensitive equipment, critical processes, and high requirements for qualification and control of facilities.
Active ingredient manufacturers
Chemical or biological production sites manufacturing active substances, where industrial equipment maintenance and process safety are essential for production continuity.
AQ Manager CMMS, the benchmark for the pharma industry
Our maintenance software is designed to integrate easily into your environment and with your teams in the field.
Model your own maintenance and quality processes, in line with your GMP requirements and internal standards.
Our client cases in the sector
AQ Manager CMMS vs. a classic CMMS
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Frequently asked questions
A CMMS, or Computerized Maintenance Management System, centralizes and optimizes all maintenance tasks, regardless of the field of activity. It gathers information on equipment, organizes preventive and corrective actions, monitors spare parts stock levels, and maintains a detailed record of each intervention. In the pharmaceutical sector, it performs an additional function by recording actions taken on certified equipment and providing the traceability required by standards such as GMP or 21 CFR Part 11.