GMP-compliant design for API plants, biotech & pharma facilities across India, Africa & Middle East.
Established 2004 · Pune, India · Single-window turnkey pharma engineering firm. GMP-compliant design from concept to commissioning.
Years of Experience
Greenfield Projects
Brownfield Projects
Consultants
End-to-End Architecture, Industrial Planning & Project Management
Master planning, concept design, working drawings, residential, commercial and industrial architecture.
Factory planning, warehouses, logistics parks, production facilities and industrial campuses.
RCC, steel structures, load analysis, detailed engineering and execution support.
Municipal approvals, fire NOC, environmental clearances and compliance support.
Site coordination, contractor management, budgeting, quality checks and timelines.
Land identification, planning, design, approvals, execution and project handover.
We design warehouses, cold chain storage & material flow corridors that reduce handling time, eliminate contamination risks & ensure uninterrupted supply.
Fire safety, containment, explosion-proof zones & emergency egress built into every layout — compliant with OSHA, Schedule M & GMP standards.
Emergency exits, suppression systems, containment walls and fire-resistant infrastructure integrated into facility design.
Hazardous area classification and safety measures for solvent handling, API production and critical operations.
Pressure cascades, airlocks and controlled environments designed to eliminate contamination risks.
Regulation-compliant evacuation routes, muster points and emergency response planning.
AHUs, HEPA filtration, differential pressure, temperature & humidity control with complete qualification documentation — designed to meet ISO 14644, Schedule M, WHO-GMP and cGMP requirements.
| System Type | AHU-based centralised / decentralised with recirculation and 100% fresh air configurations. |
| Filtration | HEPA H13/H14 terminal filtration with G4/F7 pre-filters for cleanroom compliance. |
| Cleanroom Class | ISO Class 5–8 / Grade A–D as per GMP guidelines. |
| Pressure Control | Positive & negative differential pressure cascade for containment and sterile areas. |
| T/RH Control | Precise temperature and relative humidity control for pharmaceutical manufacturing environments. |
| Compliance | WHO-GMP, Schedule M, USFDA 21 CFR Part 211, EU GMP Annex 1 and ISO 14644 compliant. |
All-in-one from concept to commissioning.
WHO-GMP, USFDA, MHRA, EU — audit-ready facilities.
Supply chain efficiency built into architecture.
Containment, egress, fire & hazardous zone planning.
Full cleanroom design & qualification documentation.
400+ greenfield projects, CIPs, Lupin & more.
Portfolio
Real questions from property owners, developers, and business owners
Application of architecture & engineering principles to design GMP-compliant pharma facilities.
Warehouse layout, cold chain, material flow & quarantine zone design for supply chain efficiency.
Hazardous materials, APIs & sterile processes demand safety built into the design from day one.
Requires cleanroom classification, HEPA filtration, pressure cascade & full qualification docs.
Share your project — our team responds within 24 hours.