Cleanroom Solutions
PHOENIXX Cleanroom Solutions deliver complete contamination-controlled environments from design to validation. Our modular approach enables faster construction, easier expansion, and compliance with ISO 14644, WHO GMP, and US FDA standards for pharmaceutical, biotech, electronics, and food processing facilities.
200+
Cleanrooms Built
ISO 5-8
Classifications
98%
Client Satisfaction
Pan India
Service Network
Why Choose PHOENIXX Cleanroom Solutions?
ISO Compliant
Cleanrooms designed and built to meet ISO 14644-1 Class 5 through Class 8 requirements.
GMP/FDA Ready
Facilities compliant with WHO GMP, US FDA, and EU GMP guidelines for pharmaceutical manufacturing.
Modular Design
Pre-engineered modular systems for rapid installation, easy expansion, and future reconfiguration.
Turnkey Delivery
Complete solutions from design and engineering through construction, HVAC integration, and validation.
Products Used in This Solution
Our integrated approach combines multiple PHOENIXX products for comprehensive solutions.
Cleanroom Partitions
Modular wall systems with flush surfaces and cam-lock joints
View Product Specifications →Cleanroom False Ceiling
Walkable and non-walkable ceiling systems with HEPA integration
View Product Specifications →Cleanroom Doors
Airtight swing, sliding, and hermetic doors
View Product Specifications →Cleanroom Flooring
Seamless epoxy and PU flooring systems
View Product Specifications →Project Gallery
Our Delivery Process
Consultation & Design
Understand your process requirements, classify cleanroom zones, and develop detailed layouts.
Engineering
Structural calculations, HVAC design, air change rates, and pressure cascade planning.
Manufacturing
Factory production of partitions, ceilings, doors, and accessories with quality control.
Installation
On-site erection by trained teams with minimal disruption to existing operations.
Validation & Handover
Particle count testing, DOP testing, air velocity checks, and IQ/OQ documentation.
Application Guide
What cleanroom classifications do you build?
We design and construct cleanrooms from ISO Class 5 (Class 100) to ISO Class 8 (Class 100,000). The classification is determined by your process requirements, and we engineer the HVAC, filtration, and construction accordingly.
Are your cleanrooms suitable for pharmaceutical manufacturing?
Yes. Our cleanrooms meet WHO GMP, US FDA 21 CFR, and EU GMP Annex 1 requirements. We provide complete documentation including DQ, IQ, OQ protocols for regulatory compliance.
Can you build cleanrooms for electronics and semiconductor?
Yes. We build ESD-safe cleanrooms for semiconductor fabrication, PCB assembly, and precision electronics manufacturing with appropriate grounding, materials, and air filtration systems.
Do you handle HVAC integration?
Yes. Our turnkey approach includes complete HVAC design with AHU sizing, ductwork, HEPA/ULPA filtration, pressure cascade design, and BMS integration for automated environmental monitoring.
What Our Clients Say
“PHOENIXX delivered our ISO Class 7 cleanroom for API manufacturing ahead of schedule. The quality and GMP compliance documentation were excellent. Highly recommended.”
Frequently Asked Questions
What is the cost of cleanroom construction?
How long does cleanroom construction take?
What documentation do you provide?
Can existing facilities be converted to cleanrooms?
Do you provide maintenance services?
What HVAC systems do you use?
Ready to Start Your Project?
Our team is ready to help you plan and execute your infrastructure project with precision and reliability.