Envigaurd designs, builds and commissions turnkey cleanrooms for pharma, biotech, R&D and other regulated facilities in India. We deliver the cleanroom HVAC, MEP services, lab furniture and gas distribution as one project, so a single team is accountable from design to validation.
What a turnkey cleanroom project covers
- Cleanroom design and layout planning
- Cleanroom HVAC: air handling units, ducting and filtration, including HEPA H13 filters
- MEP contracting: mechanical, electrical and plumbing services
- Lab furniture and fit-out
- Gas distribution systems
- Exhaust ventilation and scrubber systems for process fumes
- Commissioning, validation support and annual maintenance
Standards that decide the design
Cleanroom classification follows ISO 14644-1, and pharmaceutical facilities also work to GMP grades A to D. Our guides explain how each affects the HVAC design:
- GMP cleanroom grades A, B, C and D
- ISO 14644 cleanroom classification guide
- Cleanroom HVAC: retrofit vs new build
- Pharmaceutical cleanroom HVAC validation (DQ, IQ, OQ, PQ)
Regulated lab and R&D facilities we have built
- Bioneeds India: a 14,000 sq. ft. three-story biopharma, microbiology and cell culture lab R&D facility in Tumkur, Bangalore.
- Neovantage Innovative Park, Genome Valley, Hyderabad: a 6,000 sq. ft. aseptic lab, drug intermediate lab, UF/MFU lab and fermentation R&D lab.
- CAE: a 12,000 sq. ft. aviation and defence research and training center in Whitefield, Bangalore.
- CDYMAX Pharma India: a 2,500 sq. ft. oncology, QC and general storage lab in Jigani, Bangalore.
How a turnkey cleanroom project runs
- Initial consultation to understand your requirements and goals
- Customised design for your cleanroom class and process
- Manufacture or procurement of the components
- Installation and setup by our own teams
- Monitoring and support after handover
Frequently asked questions
What is a turnkey cleanroom?
A turnkey cleanroom is delivered as one project by one contractor, from design and construction through HVAC, services, installation and commissioning. Envigaurd handles these stages together, so one team is accountable for the finished facility.
Which industries does Envigaurd build cleanrooms for?
We build for pharmaceutical, biotech, R&D, defence and other regulated facilities. Recent projects include biopharma and aseptic labs in Bangalore and Hyderabad, and an aviation and defence research and training centre.
Which standards classify a cleanroom?
Cleanrooms are classified by airborne particle limits under ISO 14644-1. Pharmaceutical facilities also use GMP grades A, B, C and D. The class you need decides the air changes, filtration and pressure design of the HVAC system.
Does Envigaurd support the cleanroom after handover?
Yes. We offer annual maintenance contracts for HVAC, exhaust and scrubber systems, so the cleanroom keeps running as designed after commissioning.
Plan your cleanroom
Tell us your cleanroom class, area and process, and our engineers will outline the scope. Contact Envigaurd or see our turnkey projects.
