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MEPF & Cleanroom EPC for Pharma & Life Sciences

In pharma, the building services are part of the product. We design and build GMP-compliant cleanroom HVAC, clean utilities, power and fire systems — validated to Schedule M, WHO-GMP and ISO 14644 — so your facility passes audit and protects every batch.

Engineered to WHO-GMP standards — cleanroom HVAC, pressure cascade and validated documentation for pharma and life-science facilities, backed by 535+ projects and a zero-incident HSE record.
  • 535+ projects
  • ISO 9001:2015 Certified
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The Challenge

What pharmaceutical & cleanroom projects demand

  • WHO-GMP / Schedule M compliance
  • Cleanroom classification & pressure cascade
  • Cross-contamination control
  • Validation & qualification (IQ/OQ/PQ)
  • Uninterrupted, monitored operation
Our Solution

What we deliver

  • Cleanroom HVAC — AHUs, HEPA, pressure cascade
  • Temperature, RH & particle control
  • HT/LT power with UPS & DG redundancy
  • Clean-agent fire suppression & detection
  • BMS/EMS monitoring & validation documentation
Overview

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.

Sub-sectors we serve

Oral solid & liquid formulationsAPI & bulk drugsSterile injectables & vialsNutraceuticals & ayurvedicBiotech & vaccinesMedical devices & diagnostics
Why Secured Engineers Pvt. Ltd.

Why pharmaceutical & cleanroom leaders choose us

Built and validated to WHO-GMP

Cleanroom HVAC designed to Schedule M, WHO-GMP and ISO 14644 — classification, air changes, HEPA and pressure cascade — with IQ/OQ/PQ validation documentation for audit.

Contamination control by design

Correct pressure cascades, room-to-room differentials, temperature and RH control and material/personnel flow engineered to stop cross-contamination before it starts.

Redundant power & clean-agent fire

HT/LT power with UPS and DG backup keeps critical areas running; clean-agent suppression and detection protect product and people without water damage.

One partner, audit-ready handover

Cleanroom HVAC, utilities, power and fire under one contract, with BMS/EMS monitoring, TAB and complete validation documentation at handover.

FAQs

Pharmaceutical & Cleanroom MEPF & solar — your questions answered

Do you design and validate cleanroom HVAC to WHO-GMP and ISO 14644?

Yes. We design cleanroom HVAC — AHUs, HEPA filtration, air-change rates, temperature/RH control and pressure cascade — to Schedule M, WHO-GMP and ISO 14644, and deliver the validation documentation (IQ/OQ/PQ) your quality team and regulators require.

What cleanroom classifications can you build?

We build cleanrooms across ISO Class 5–8 (GMP Grade A–D) for sterile and non-sterile pharma, biotech and medical-device facilities, with the correct air changes, HEPA terminals and pressure differentials for each grade.

Do you cover the full MEP scope for a pharma plant, not just HVAC?

Yes — cleanroom HVAC plus HT/LT power with UPS and DG redundancy, clean-agent fire suppression and detection, plumbing and clean-utility support, and BMS/EMS monitoring, from design and approvals to testing, balancing and validation.

Which pharma regions do you serve?

We serve pharma clusters across India — including the Baddi–Barotiwala–Nalagarh belt, Punjab, Delhi NCR, Gujarat and the South — with our corporate office in Noida and registered head office in Ludhiana.

Planning a pharmaceutical & cleanroom project?

Get a free consultation and quote. We design, take all approvals, and execute — you stay stress-free.

ONE PARTNER. END TO END. You focus on your business — we handle the rest.
Quality Safety Commitment
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