
Modular Cleanroom
- ISO Classes 1-9 available
- Modular adaptable design
- cGMP compliant construction























ISO Certified
GMP Compliance
ACH Engineering offers comprehensive pharmaceutical cleanroom solutions including modular walls, ceilings, doors, vision panels, and complete turnkey installations. Our prefabricated cleanroom components meet ISO classifications and cGMP requirements, delivering faster installation and cost-effective controlled environments for pharmaceutical manufacturing, compounding pharmacies, and biotechnology facilities across North America.
Talk to our experts for custom solutions and tailored guidance.
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What ISO classifications do ACH Engineering cleanrooms meet?
Our modular cleanrooms meet ISO Classes 1-9 depending on your pharmaceutical manufacturing requirements, ensuring compliance with industry standards.
How long does it take to install a pharmaceutical cleanroom?
Are ACH cleanrooms compliant with FDA and cGMP regulations?
Can modular cleanrooms be expanded or reconfigured later?
What materials are used in pharmaceutical cleanroom construction?
Do you provide turnkey cleanroom installation services?
What maintenance is required for modular pharmaceutical cleanrooms?
Talk to our experts for custom solutions and tailored guidance.

ISO-classified cleanrooms for drug manufacturing, tablet production, and sterile filling operations meeting cGMP standards.

Controlled environment solutions for biotech research, cell culture labs, and GMP-compliant containment areas.

USP <797> and <800> compliant cleanrooms for sterile and hazardous drug compounding with proper segregation.

ISO-classified assembly cleanrooms for medical device production ensuring sterility and contamination control.
Talk to our experts for custom solutions and tailored guidance.



Prefabricated cleanroom components enable faster installation, easy expansion, and reconfiguration to adapt to your evolving pharmaceutical manufacturing needs without facility disruption.
Our cleanroom solutions meet ISO classifications, cGMP requirements, and FDA regulations with comprehensive validation services ensuring your pharmaceutical operations maintain full compliance.
From initial design through validation, our experienced team manages every aspect of your cleanroom project delivering on-time, within-budget pharmaceutical solutions across North America.
Connect with our cleanroom specialists for expert guidance on ISO-classified pharmaceutical solutions. Expect a detailed response within 24 hours.
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