Our journey in pharmaceutical project consultancy began in 2004 with a strong belief in disciplined planning and regulatory clarity. Our first green field project was Titan Laboratories in Mahad, Maharashtra, developed for modified release drug delivery systems. That facility achieved approvals from EU GMP, Korean FDA, and TGA Australia, reflecting structured execution and regulatory alignment. Since then, we have undertaken multiple green field and upgradation projects for API and formulation manufacturing units. Each project strengthens our commitment to building compliant, efficient, and inspection-ready pharmaceutical facilities.

We begin every project with a clear conceptual design and master planning. A strong foundation prevents costly redesign and compliance delays later. We assess product type, regulatory pathway, and process flow before defining layout strategy. This ensures space planning aligns with GMP expectations and operational efficiency. Early planning reduces risk during validation and authority inspections. Our structured design approach supports smooth regulatory approvals across global markets.

Our services include architectural and interior design aligned with cleanroom standards and GMP zoning principles. We coordinate civil, mechanical, and electrical planning with production requirements. HVAC systems, controlled environments, and piping utilities are designed to support contamination control and product integrity. Effluent and water treatment systems are planned with regulatory and environmental compliance in mind. Every technical decision connects directly with regulatory approval expectations.