01
Conceptual & Basic Design
Feasibility studies, facility concepts, and basis-of-design that align capacity, compliance, and capital from the outset.
Read More
From conceptual design through commissioning and qualification — specialized EPCm engineering for the pharmaceutical and life-sciences sector.
Feasibility studies, facility concepts, and basis-of-design that align capacity, compliance, and capital from the outset.
Multidiscipline detailed design — architectural, process, mechanical, electrical, and automation — coordinated to one model.
Compliance strategy, risk assessment, and validation planning built to cGMP expectation and inspection readiness.
Classified cleanrooms and HVAC engineered for contamination control, pressure cascade, and ISO-class stability.
Process systems and clean utilities — WFI, PW, clean steam, and gases — designed for purity, capacity, and control.
Structured C&Q — IQ, OQ, PQ — that carries the design intent through to a documented, qualified handover.
We treat regulatory expectation as a design input from day one — risk is assessed early, and every system is specified so that qualification confirms the design rather than repairs it.
Quality risk management embedded from concept.
Design intent traceable through to qualification.
Contamination control and data integrity by design.
Inspection-ready documentation at every stage.