A cleanroom is a controlled environment designed to minimize the presence of airborne particles, contaminants, and pollutants. These rooms are essential in industries where even microscopic impurities can compromise research, manufacturing, or testing outcomes.
Cleanrooms are classified based on the number of particles per cubic meter. For example:
• ISO 1: Most stringent (used in nanotech)
• ISO 5: Aseptic areas (biotech/pharma)
• ISO 7 & 8: Less stringent (packaging, assembly)
Unlike a standard lab, a cleanroom maintains strict controls over air quality, temperature, humidity, pressure, and particulate levels—ensuring sterile and contamination-free conditions necessary for sensitive work.
Modular cleanrooms use prefabricated panels and are faster to install and modify. Conventional cleanrooms use brick-and-mortar or drywall construction and are typically used for large-scale or permanent facilities.
Project & Services
Yes, we offer complete turnkey services—covering design, layout, HVAC, utility integration, validation, documentation, equipment procurement, and final commissioning.
Absolutely. We provide retrofitting services to improve existing facilities by upgrading HVAC systems, equipment, layouts, and compliance standards—while minimizing downtime.
Yes, we offer comprehensive consulting to ensure adherence to ISO 14644, WHO-GMP, US FDA, and other relevant regulatory standards. We also help prepare documentation and support audit readiness.
Timelines vary by scope and classification, but most standard cleanroom projects are completed within 8 to 16 weeks, including design, execution, and validation.
Our validation services include particle count testing, air velocity tests, recovery tests, filter integrity testing, pressure differentials, temperature & humidity monitoring, and final certification.
Industries & Applications
Yes, we’ve worked with agencies like ISRO, DRDO, and BARC, delivering cleanrooms for R&D, electronics assembly, and secure laboratories with stringent compliance and documentation.
Yes, we design and build Biological Safety Level (BSL-2 and BSL-3) labs with appropriate containment, pressure zoning, airlocks, and decontamination protocols.
Yes, we have delivered cleanroom and lab projects for leading Indian institutes such as IITs, NITs, Central Universities, and other research bodies focused on nanotechnology, biotech, and electronics.
Technical & Equipment
We recommend cleanroom-specific HVAC systems with HEPA/ULPA filters, 100% fresh air or recirculation units, dedicated AHUs, and controls for temperature, pressure, and humidity.
HEPA filters should be tested annually (or semi-annually in critical applications) and replaced based on performance, typically every 3–5 years or as per validation results.
Yes, we help with selection, procurement, and installation of equipment like pass boxes, laminar air flow units, biosafety cabinets, and cleanroom-grade workstations and seating.
Yes, we offer electrostatic discharge (ESD) protection including ESD-safe flooring, workbenches, grounding systems, and protocols for sensitive electronic component manufacturing.
Our validation services include particle count testing, air velocity tests, recovery tests, filter integrity testing, pressure differentials, temperature & humidity monitoring, and final certification.
Support & Maintenance
Yes, we offer customizable AMCs for HVAC systems, equipment calibration, and cleanroom maintenance to ensure long-term reliability and compliance.
We provide on-site and remote training programs covering cleanroom behavior, contamination control, gowning protocols, SOP compliance, and audit preparation.
Yes, we develop and deliver custom SOPs, visual protocols, and safety manuals that are aligned with your facility and regulatory requirements.
Yes, we assist clients during audits by reviewing documentation, validating systems, and providing technical explanations to auditors when needed.
