Enhancing Manufacturing Productivity to Quickly and Cost-effectively Deliver Products

Drug patent expirations, greater customer expectations, less productive pipelines, stringent regulatory requirements and industry consolidation are just a few factors that are placing immense pressure on life sciences organizations. These companies are focused on accelerating internal R&D productivity, reducing risk and increasing profit margins. In an effort to meet these demands, these organizations focus on efficient asset management and implement Enterprise Asset Management (EAM) solutions. Therefore, they partner with industry experts that help them quickly and cost-effectively bring enhanced products to market.

Qualtech Systems, the industry’s premier Maximo implementation partner, has helped numerous life sciences organizations increase profitability through optimizing asset performance, reducing compliance related costs and leveraging current IT investments. Whether you are trying to meet FDA 21 CFR Part 11 regulations, create Compliance Assistance Documentation for validation projects, improve capital asset utilization or integrate to your existing ERP solution, our industry experts have been there and can help your company succeed.

We understand the challenges associated with meeting the FDA, the International Organization for Standardization (ISO) and other regulatory bodies’ requirements. Our team has direct experience implementing your industry’s maintenance best practices, and has provided unparalleled support for instrument calibration and asset-related Corrective Action and Preventive Action (CAPA) processes. Our seasoned consultants immediately add value, and have helped your industry peers enhance their overall manufacturing productivity while reducing operational risk. Join other life sciences companies in leveraging our technical and industry knowledge. Contact us to learn more about how we can help with your specific needs.

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