MEPF & Cleanroom EPC for Pharma & Life Sciences

India's trusted pharmaceutical & cleanroom MEPF & solar EPC partner

Secured Engineers Pvt. Ltd. is an MEP and cleanroom EPC contractor for pharmaceutical, API and life-science facilities across India — including the Baddi–Barotiwala–Nalagarh pharma belt, Punjab and Delhi NCR. We design, execute and validate the cleanroom HVAC, clean utilities, power and fire systems that a GMP facility depends on, under one accountable contract.

In a regulated facility, the HVAC system is a critical control. Room classification, air-change rates, HEPA filtration, temperature, humidity and a correctly designed pressure cascade are what keep product sterile and audits clean. Our engineers design to WHO-GMP, Schedule M and ISO 14644, and deliver the validation documentation — IQ/OQ/PQ — that your quality team and the regulator require.

We handle the full building-services scope — cleanroom AHUs and ducting, HEPA terminals, BMS/EMS monitoring, HT/LT power with UPS and DG redundancy, clean-agent fire suppression, and clean-utility support — from design and statutory approvals through installation, testing, balancing and qualification. One team owns the envelope's engineering so your facility is built right, validated, and ready for inspection.

Choosing a cleanroom contractor in India means deciding which half of the room you are buying first. One kind of vendor makes the envelope — modular partitions, panels, doors, pass boxes — and fits it out. The other engineers what makes the room a cleanroom: the air. Classification and air-change rates, HEPA filtration, the pressure cascade between grades, temperature and humidity control, and the qualification documentation that proves all of it held. We are the second, and we say so rather than claiming both, because the risk in a GMP facility does not sit in a panel joint. It sits in a cascade that reverses when a door opens, an AHU that cannot hold humidity through a Baddi monsoon, or a validation pack a regulator will not accept. Where the envelope is a specialist package we coordinate to it; where the client wants one contract, we carry the services scope and the interface with it.

Settle the regulatory basis before design, not during audit. We design to ISO 14644 classification and the GMP requirements applicable to the facility — and note that Schedule M has been revised, so the text in force and the timeline applying to your unit must be confirmed against CDSCO's current notification rather than assumed from an older build. Where a facility is being engineered for a particular regulator, the pressure regime, the monitoring and the documentation are built to that standard from the start; retrofitting them to an already-qualified room is the expensive route.