Clean manufacturing facility projects are constantly challenged by their need to meet critical time-to-market schedules and demanding high-purity manufacturing standards. O'Brien & Gere's Capital & Facilities Solutions (CFS) Business Unit designs and builds clean manufacturing facilities to challenging standards under fast-track schedules to support the production of clean, zero defect products.

Our 360° Project Execution Process™ for clean manufacturing facilities such as API, Biologics Production, Pharmaceutical Dosage Form, Electronics, and Consumer Products addresses the following unique challenges by:

• Achieving zero unplanned interruptions to existing operations
• Maintaining clean construction/contaminant control protocols
• Meeting regulatory compliance requirements (FDA, USDA, ISO, EU) Offering single-source responsibility, O'Brien & Gere's CFS Business Unit has the ability to conceptualize, design, build, install, commission, and qualify a wide range of clean manufacturing facilities. We offer tailored contracting arrangements to meet the business needs of our clients, including guarantees for schedule, cost, quality, and facility performance.
• Containing & controlling potent compounds