Cleanroom & controlled environment engineering

Environments held to zero compromise.

CONDESCE designs, builds, and validates cleanrooms and controlled environments for pharma, biotech, healthcare, and semiconductor facilities — from first layout sketch to commissioning documentation.

Designed to EU-GMP ISO 14644 WHO-GMP USFDA
++ Core competencies

Five disciplines, one controlled outcome.

Every facility we deliver moves through the same disciplines — space planning, sustainability, contamination control, industry-specific engineering, and turnkey delivery — so nothing is handed off without accountability.

Smart Lab Designs

  • Integrated space planning & modular construction
  • Enhanced workflows with automation
  • Ergonomic, digital-first environments

Sustainable Infrastructure

  • Eco-friendly, durable materials
  • Energy-efficient HVAC systems
  • Waste & resource management

Compliant Cleanroom & Controlled Environments

  • EU-GMP, ISO 14644, WHO-GMP, USFDA designs
  • Built for aseptic processing & biosafety
  • Ready for validation and audit

Industry-Focused Solutions

  • Pharma — R&D, QC labs, production cleanrooms
  • Biotech — bioreactor & tissue culture labs
  • Healthcare — pathology & diagnostics
  • Semiconductors — ISO Class 5–8 cleanrooms

Turnkey Execution & after sales Support of Cleanrooms

  • Concept-to-commissioning services
  • Design, HVAC and IOTs
  • Qualification & regulatory documentation
0 Compliance baseline

Contamination control isn't a feature. It's the pressure cascade.

Cleanrooms hold their integrity through engineered air — unidirectional flow, HEPA/ULPA filtration, and pressure differentials that keep contamination moving in one direction only: out.

Air conditioning schematic for semiconductor cleanrooms showing unidirectional vertical airflow through HEPA/ULPA filters
Cleanroom cutaway diagram showing pressure cascade of ++, +, and 0 between adjoining rooms
Exploded diagram of modular cleanroom panel construction showing ceiling panel, air duct, sliding door, window, air shower and pass box
EU-GMP — Annex 1 aseptic processing
ISO 14644 — particulate classification
WHO-GMP — pharmaceutical manufacturing
USFDA — validation & audit readiness
+ Industry focus

Built around what each industry can't compromise on.

The same cleanroom principles read differently depending on what's inside the room — a QC lab, a bioreactor suite, a diagnostics bench, or a wafer line.

01 — LIFE SCIENCES

Pharmaceuticals

Drug manufacturing, R&D, and quality-control laboratories.

02 — LIFE SCIENCES

Biotechnology

Bioreactor and tissue-culture labs with tight contamination control.

03 — INDUSTRY

Semiconductors & Electronics

ISO Class 5–8 cleanrooms for microelectronics assembly.

04 — HEALTHCARE

Healthcare

Pathology, diagnostics, and sterile compounding spaces.

+ Indoor growing

Clean room greenhouses.

A hybrid facility that pairs plant-growth environments with the cleanroom standards used across pharma, biotech, and semiconductor work — precise control over temperature, humidity, and contamination, enabling cultivation of sensitive or high-value plant species under GMP-like conditions.

Clean air-supplied greenhouses Laboratories up to BSL-3 Clean rooms
++ Turnkey delivery

From concept sketch to commissioning binder.

One point of accountability across design, construction, and qualification — so the facility that gets validated is the one that was actually promised.

Modular panel-built controlled environment room with sliding doors and integrated shelving Cleanroom technician in full protective suit working at a sterile workstation
01

Design & engineering

Space planning, HVAC and electrical layout, panel and modular construction drawings.

02

Supply, install, test, commission

Modular panels, HVAC, HEPA filtration systems, BMS and furniture — installed and commissioned on site.

03

Validation & documentation

QA/QC documentation aligned to ISO 14644, GMP, and EU/FDA standards, ready for audit.

04

Post-sale support

Annual maintenance contracts to keep pressure differentials, filtration, and controls in spec.

0 Reference standards

Design & safety guidelines for laboratory infrastructure.

Every layout is checked against the same reference standards before it reaches a client's desk.

Design and safety guidelines reference diagram for laboratory infrastructure

Planning a cleanroom or controlled environment?

Tell us the industry, the scale, and the compliance target — we'll come back with a layout and a scope, not a sales pitch.

Write to bd@condesce.com →

Call +91 99723 99088