Expert Cleanroom Services – Engineered for Perfection
Services We Offer
At Sri Modular Clean Rooms, we specialize in delivering end-to-end cleanroom solutions tailored to meet the highest industry standards. Our services include cleanroom design, modular construction, HVAC integration, validation, and maintenance—ensuring controlled environments for pharmaceuticals, electronics, biotechnology, and other precision-driven industries. With a focus on quality, compliance, and customization, we help you create cleanroom spaces that are efficient, scalable, and future-ready.
Annual Maintenance Contract (AMC)
Support & Technical help desk after sales
Upgrading of Equipment’s
Prompt response for repairs
Spare replacement of clean room equipment’s and medical devices.
Principles of Clean Room Validation
A cleanroom is a modular environment in which the following environmental factors are kept under control; temperature, airborne particulates, microbes, relative humidity, differential pressure, and air flow.
Cleanroom Validation is performed for a variety of reasons. To ensure that the design of the facility is fit for its intended purpose; to ensure that the facility, equipment, and environment meets User Requirement Specifications (URS); to ensure that the facility, equipment, and environment meet defined regulatory requirements; to ensure that the facility, equipment, and its environment function together as a system to meet defined standards.
Cleanrooms are validated and then certified to a chosen class of ISO 14644-1. Each class of ISO14644-1 has its unique requirements that must be made for a facility to be classified in the specified classification.
Tests:
- Particle Count Test
- Air Velocity Test
- HEPA Integrity Test (D.O.P)
- Recovery Test
- Differential Pressure Test
- Air Flow Pattern
- Noise Level Test
- Temperature & RH Test
- Light Intensity Test
Standards:
- ISO 14644-1
- US FED STD 209 E