
Cleanroom Modular Walls
- Adaptable modular construction
- ISO Class 1-9 classifications
- Fast installation timeline




















PEO Certified
PMI Member
ISPE Member
Class 1000 Cleanrooms with Instrument Assembly Services deliver ultra-clean controlled environments for precision manufacturing and assembly operations. These ISO Class 6 equivalent facilities feature modular walls, specialized coving, flush doors, and vision panels designed to maintain stringent particulate control. Engineered for pharmaceutical, medical device, electronics, and aerospace applications, our turnkey solutions include validation services and custom laboratory furniture to support your critical assembly and testing requirements.
Talk to our experts for custom solutions and tailored guidance.
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What ISO classification does a Class 1000 cleanroom meet?
A Class 1000 cleanroom corresponds to ISO Class 6, allowing a maximum of 1,000 particles (0.5 microns or larger) per cubic foot of air.
How long does it take to install a modular Class 1000 cleanroom?
Can Class 1000 cleanrooms be expanded or reconfigured later?
What industries commonly use Class 1000 cleanrooms for assembly?
Are ACH Engineering cleanrooms cGMP compliant?
What types of doors are available for Class 1000 cleanrooms?
Do you provide validation services after cleanroom installation?
Talk to our experts for custom solutions and tailored guidance.

Sterile compounding, manufacturing, and quality control labs requiring ISO Class 6 environments for drug production.

Precision assembly and testing of implantable devices, surgical instruments, and diagnostic equipment in controlled environments.

Microchip fabrication, circuit board assembly, and ESD-safe testing areas for sensitive electronic component manufacturing.

GMP labs, cell culture rooms, and sterile processing areas for biotech R&D and containment operations.
Talk to our experts for custom solutions and tailored guidance.



End-to-end project management from design through validation by highly qualified engineers ensures seamless cleanroom delivery on schedule and within budget.
Prefabricated cleanroom components enable faster installation, easy expansion, and cost savings compared to traditional construction methods.
Deep understanding of ISO, cGMP, FDA, and USP standards ensures your cleanroom meets all regulatory requirements for pharmaceutical and medical device manufacturing.
Our cleanroom engineering experts will respond within 24 hours with a tailored solution for your instrument assembly requirements.
For immediate assistance, feel free to give us a direct call at +1 647-406-5721 You can also send us a quick email at sales@achengineering.com
For immediate assistance, feel free to give us a direct call at +1 647-406-5721 You can also send us a quick email at sales@achengineering.com