Pharmaceutical Facility Architecture · Since 2009
Where Air Becomes
Infrastructure
ISO 5 · ISO 7 · ISO 8 · cGMP · Gene Therapy · Fill-Finish · HVAC
Facility Zones
Walk the Floor Plan
Each card is a zone. Open any to see cross-section airflow diagrams, pressure cascades, and classification specifications. The complexity reveals itself only on demand.
01
Gowning Suite
ISO 7 / Grade CThe threshold between uncontrolled and controlled environments. Sequential pressure differentials enforced at every garment layer.
02
Fill-Finish Line
ISO 5 / Grade AAseptic filling under Class 100 laminar flow. The most critical zone in any sterile manufacturing facility.
03
QC Laboratory
ISO 8 / Grade DAnalytical testing environment. Negative pressure containment for potent compounds. Segregated from manufacturing flow.
04
HVAC Mechanical Penthouse
Utility / GMP CriticalThe invisible engine. Air handling units, chilled water loops, and HEPA terminal banks that govern every breath inside the facility.
05
Transfer Corridor
ISO 8 / Grade DMaterial flow choreography. Pass-through chambers and dynamic air curtains that move product without moving contamination.
GMP Facilities Delivered
Sq Ft Classified Space
ISO Classifications Designed
On-Time Commissioning Rate
Countries Regulated
How We Design
The Invisible Made
Rigorous
Pharmaceutical facility design is not architecture with compliance bolted on. It is compliance expressed through architecture. Our process begins with the regulatory framework and works outward to the walls.
Facility Programme
We map your manufacturing intent against regulatory frameworks — FDA 21 CFR, EU GMP Annex 1, ICH Q10. Every design decision traces back to a compliance rationale, not an aesthetic preference.
Pressure Architecture
Cascade diagrams are not afterthoughts. We design pressure differentials as the primary structural logic — rooms, corridors, and airlocks sized around airflow before walls are drawn.
Contamination Control Strategy
A written CCS precedes every drawing package. Personnel flows, material routes, waste streams, and equipment corridors are choreographed to prevent cross-contamination at the architectural level.
Qualification Readiness
We design for IQ, OQ, and PQ from day one. HVAC validation protocols, smoke studies, and environmental monitoring plans are authored in parallel with construction documents.
Who We Architect For
Biotech COO
Scaling from 200L pilot to 2,000L commercial. First aseptic fill suite. FDA pre-approval inspection in 18 months.
VP Engineering, Pharma
Retrofitting 1980s tablet plant for gene therapy. Existing HVAC cannot support ISO 5. Concrete cannot be moved.
CDMO Founder
Bare concrete shell. No HVAC. No classified space. Full GMP facility in 24 months for first client contract.
