Compounding Cleanroom Solutions 

Compounding Facilities Built for Compliance, Safety, and Operational Precision

Designing and delivering controlled environments that support sterile compounding, hazardous drug handling, and regulatory compliance with confidence.

Ready when you are.

Why Compounding Facilities Matter

Compounding facilities require rigorous environmental control to protect sterile drug preparation, ensure patient safety, and meet stringent regulatory standards. These spaces must optimize contamination control, airflow, and access protocols to safeguard both product quality and personnel. 

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Regulatory Compliance:
Built to meet USP <797>, <800>, ISO 14644 and state and federal requirements.
Stable Temperature:
Flexible and Adaptable suites
Contamination Control:
HEPA filtration, controlled access, and cleanroom air quality.
Operational Efficiency:
Designed for Material Flow, Process Flow, People Flow

With our agnostic approach we select best architectural assembly for mechanical designs or units to achieve project, Drivers, Schedules, Cost and Quality goals.

Our Approach: 

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1
Needs Assessment & Regulatory Roadmap.
2
Provide the best options (Modular hardwall vs soft wall).
3
HVAC and airflow control.
4
Risk mitigation

Core Services

From concept through certification, we deliver comprehensive services for compounding facilities: 

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Design + Engineering
Custom layouts, risk analysis, and specification development.
Construction + Integration
Modular cleanroom build, architectural finishes, and mechanical systems.
Commissioning + Validation Support
Testing, verification, and documentation to support USP compliance.
Maintenance + Lifecycle Services
Preventive care, quarterly service, and response programs.

Unique Needs of Compounding Operations 

Addressing the Unique Needs of Compounding Operations

Compounding facilities face multiple challenges, including sterile processing environments, hazardous drug segregation, and evolving regulatory scrutiny. Precision Environments anticipate these challenges and integrate solutions that minimize downtime, reduce risk, and protect product integrity. 

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  • Maintaining pressure differentials in buffer and ante areas
  • Workflow layout for aseptic processing
  • Filtration and particulate control
  • Cleanroom certification readiness

Compliance + Standards 

Built to Meet Pharmaceutical Standards 

With over 30 years of controlled environment innovation, Precision Environments brings unmatched expertise in nanotechnology applications and ultra-clean manufacturing requirements. Our turnkey project delivery approach minimizes risk while maximizing value through our extensive supplier network and proven methodologies. We guarantee that all cleanrooms meet applicable regulatory requirements and performance specifications, backed by 24/7 emergency support services to make sure your compounding facility is up to FDA standards.

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Our compounding cleanrooms are engineered to align with current regulatory expectations, including USP <797>, USP <800>, and applicable state board guidelines. Standard operating procedures and turnover documentation support ongoing compliance.

Let’s discuss your next project