1
Consultation
Understanding your requirements and conducting feasibility studies
IV & Chemotherapy Preparation Rooms
Get Expert ConsultationSterile Compounding
ISO-classified enclosures and controlled workflows for safe IV and hazardous drug preparation
Staff & Patient Protection
Negative pressure, containment, and ergonomic design to limit exposure to cytotoxic agents
Regulatory Alignment
Designed around USP, cGMP, and local pharmacy compounding requirements
Validated Operations
From design through commissioning, documentation, and staff readiness
Engineered Compounding Environments
We design and build IV and chemotherapy preparation rooms that meet the highest standards for sterile compounding and hazardous drug handling. Every project integrates architecture, HVAC, finishes, and pharmacy equipment into a cohesive, audit-ready facility.
IV & Chemotherapy Preparation Environments
Dedicated compounding rooms protect patients from contamination and medication errors while shielding pharmacy staff from hazardous drugs. We engineer layouts, airflow, and finishes as an integrated system — not isolated equipment — so every preparation step occurs inside a validated, auditable environment. Our teams coordinate architectural, HVAC, and pharmacy workflow requirements from concept through handover.
ISO Class 5 primary engineering controls
Segregated hazardous and non-hazardous zones
Ergonomic preparation stations
Containment & Negative Pressure Control
Chemotherapy and other hazardous drug preparation demands reliable containment. We specify pressure cascades, monitoring, and alarm strategies that maintain protective airflow during normal operation and transient events such as door cycles or equipment maintenance. Surfaces, seals, and pass-through interfaces are detailed to support validated cleaning and wipe-down protocols.
Negative pressure protection
Continuous pressure monitoring
Ante-room and buffer design
Materials, Finishes & Equipment Integration
Non-porous, cleanable finishes with coved transitions reduce retention zones where residues can accumulate. We integrate biosafety cabinets, compounding isolators, storage, and waste handling into logical flow paths that support USP-aligned standard operating procedures. Medical gases, electrical, and data services are coordinated so equipment placement matches how pharmacists actually work.
Seamless, washable wall and floor interfaces
Integrated primary engineering controls
Waste and staging zones
Commissioning, Qualification & Training
We support IQ/OQ documentation, airflow visualization, and environmental monitoring plans that satisfy internal quality teams and external auditors. Training covers room use, pressure awareness, and emergency response so staff operate confidently on day one. Ongoing support helps you maintain classification and respond to layout or volume changes over time.
Validation-ready documentation
Staff orientation and SOP alignment
Lifecycle technical support
Complete System Integration
Our compounding room solutions unite containment, MEP systems, finishes, and equipment into one validated operational environment.
- Materials & Finishes
Pharmacy-grade surfaces and joints designed for frequent decontamination
- HVAC & Pressurization
Qualified airflow, filtration, and cascade control
- Equipment Integration
Isolators, cabinets, storage, and waste systems
- Training & Support
Commissioning support and staff readiness programs
Project Process
1
Assessment
Workflow, volume, and regulatory scope review
2
Design
Layout, HVAC, and containment specification
3
Implementation
Build, install, and integrate systems
4
Validation
Testing, documentation, and certification
5
Training
Staff handover and operational readiness
How We Work
A proven methodology from concept to completion
2
Design
Detailed engineering plans, compliance documentation, and approvals
3
Execution
Professional installation, construction, and system integration
4
Commissioning
Testing, validation, training, and ongoing support services
