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Advanced Features

Our clean room partition systems incorporate cutting-edge technology and design principles for optimal performance.

HEPA Filtration Integration

Seamless integration of HEPA/ULPA filtration systems for particle control down to 0.3 microns, ensuring ISO class compliance.

Antimicrobial Surfaces

Proprietary antimicrobial coatings that inhibit bacterial growth, maintaining sterile conditions for sensitive applications.

Modular Design

Flexible modular components allow for easy reconfiguration, expansion, or relocation as your facility requirements evolve.

Pressure Control

Advanced differential pressure maintenance systems ensure proper airflow direction and contamination control.

Premium Materials

We use only the highest quality materials engineered for clean room environments.

Powder Coated Steel

Durable, corrosion-resistant steel with electrostatic powder coating for easy cleaning and chemical resistance.

Tempered Glass

Safety-tempered glass panels with anti-static coatings for visibility while maintaining environmental integrity.

PVC Membranes

Seamless, non-porous PVC membranes that prevent microbial growth and are easily decontaminated.

Stainless Steel

Medical-grade 304 and 316 stainless steel for critical areas requiring maximum corrosion resistance.

Industry Applications

Serving diverse industries with specialized clean room solutions.

Pharmaceuticals

Sterile manufacturing, aseptic filling, and API production facilities meeting cGMP requirements.

Biotechnology

Cell culture labs, fermentation suites, and biosafety level laboratories for cutting-edge research.

Electronics

Semiconductor fabrication, microelectronics assembly, and nanotechnology clean rooms.

Healthcare

Operating theaters, sterile processing departments, and compounding pharmacies.

Compliance & Standards

Our systems meet and exceed international clean room standards and regulations.

ISO 14644

Fully compliant with ISO 14644-1 through -9 standards for cleanroom classification and monitoring.

GMP Compliance

Designed to meet current Good Manufacturing Practice requirements for pharmaceutical applications.

FDA Guidelines

Adherence to FDA regulations for medical device manufacturing and sterile products.

Key Benefits

Why choose our clean room partition systems for your facility.

Rapid Installation

Modular design enables faster installation with minimal disruption to ongoing operations.

Enhanced Safety

Built-in safety features and fail-safe mechanisms protect both products and personnel.

Cost-Effective

Reduced energy consumption and maintenance costs with optimized airflow design.

Our Process

From consultation to commissioning, we ensure a seamless project execution.

Consultation

Needs assessment and feasibility study.

Design

Custom engineering and 3D modeling.

Fabrication

Precision manufacturing in controlled facility.

Installation

Certified installation and commissioning.

Frequently Asked Questions

Find answers to common questions about our clean room solutions.

What is the typical lead time for a clean room installation?

Lead times vary based on project complexity and size. Standard modular clean rooms can be installed in 4-8 weeks, while larger custom facilities may require 12-20 weeks from design approval to commissioning. We provide detailed project timelines during the consultation phase.

Can existing facilities be upgraded to higher clean room classes?

Yes, we specialize in facility upgrades and retrofits. Our modular partition systems can often be integrated into existing structures. We conduct comprehensive assessments to determine feasibility and provide upgrade paths to achieve higher ISO classifications.

What maintenance is required for clean room partitions?

Our systems require minimal maintenance. Recommended periodic activities include: visual inspections for seal integrity, cleaning with approved disinfectants, filter replacements per manufacturer schedule, and verification of pressure differentials. We provide comprehensive maintenance guides and offer service contracts.

Do you provide validation and certification services?

Yes, we offer full validation packages including IQ/OQ/PQ documentation, particle count testing, air velocity and uniformity verification, pressure differential mapping, and certification to ISO 14644 standards. All documentation is provided for regulatory submissions.

Clean Room Partition Systems