United Pharmaceuticals Inc. utilizes purpose-built manufacturing machinery and processing equipment designed to support controlled, consistent, and scalable pharmaceutical operations. All equipment is selected based on process suitability, compliance requirements, and operational reliability. Equipment qualification activities ensure systems perform as intended and support reproducible outcomes across defined operating parameters.
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All critical machinery is subject to structured validation protocols to confirm performance, accuracy, and repeatability. Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities are conducted in accordance with established validation plans.
Documented validation ensures equipment remains fit for use throughout its lifecycle while supporting regulatory compliance and process integrity.
A defined preventive maintenance program is implemented to maintain equipment functionality and reduce the risk of unplanned downtime. Scheduled inspections, calibration, and servicing activities are performed to ensure consistent operational performance. Maintenance records are controlled and reviewed to support traceability and audit readiness.
Machinery and equipment performance is continuously evaluated through defined operational checks, routine monitoring, and controlled performance reviews. Key parameters, deviation trends, equipment wear indicators, and functional variances are assessed to identify potential risks and initiate timely corrective or preventive actions.
This structured oversight ensures sustained equipment reliability, minimizes operational disruptions, and supports safe, compliant, and efficient pharmaceutical manufacturing throughout the equipment lifecycle.
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