MatterGuard®

Cleanroom Construction

Turnkey Controlled Environments

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About MatterGuard® Cleanrooms

Hardwall cleanrooms designed, built, and installed by AVM Group

AVM Group designs and builds modular hardwall cleanrooms that deliver consistent environmental control for manufacturing, laboratory, and regulated facilities.

Each cleanroom is engineered around your classification requirements, equipment layout, and existing building conditions for consistent performance.

Common Cleanroom Industries

Pharmaceuticals and Biotechnology
Semiconductor and Microelectronics Manufacturing
Medical Device Manufacturing
Injection Molding and Technical Plastics
Circuit Board Printing and Electronics assembly
Optical, LED, and Coated Surface Manufacturing
Metrology and Measurement labs
Quality Inspection and Inclusion Detection
Institutional and Educational

Cleanroom Features and Specifications

CLEANROOM INTEGRITY & CONTAINMENT

Designed to control particulates while maintaining engineered and designed specifications for pressure differentials, temperature, and humidity.

OPERATION & USE

Planned around personnel and staff occupancy, material, and equipment movement to avoid airflow imbalance, dead zones, and workflow bottlenecks.

CONSTRUCTION MATERIALS

Built from non-shedding, cleanable materials selected for classification level, chemical exposure, cleaning frequency, required insulation, and electrostatic discharge (ESD) properties if applicable.

Seismic / Structural

Engineered options available to provide minimum required support for cleanroom components to structural decks for additional floor space and storage mezzanines.

MatterGuard® Product Specifier

Quickly identify the ideal solution based on your facility’s ISO cleanroom classification, process needs, and operational objectives.

What sets MatterGuard® Cleanrooms apart

Protect with precision. Customize for your needs. Install with confidence.

Predictable Room Performance

Cleanrooms by AVM Group are built to maintain stable airflow, pressure, and cleanliness levels throughout normal operation.

Validation Without Surprises

Validation requirements are addressed during design so certification follows the build without delays and minimizes field changes.

Built Around Your Process

Each room is planned around your equipment, workflows, and day-to-day use.

MatterGuard® Cleanroom Components

Cleanrooms consist of the envelope, the mechanical system(s), and the control system.

As part of our cleanroom design-build process, we work with a variety of component manufacturers to assemble the best solution for your specific application.

Inside of a cleanroom facility with two pass-throughs

Cleanroom Envelope

Defines the controlled space, including walls, ceilings, flooring, doors, and glazing, with sealed interfaces that maintain room integrity during normal use

Control System

Monitors room conditions and allows adjustments during operation to keep the environment within required limits

Pass-Through (optional)

A controlled gateway that facilitates the safe and contamination-free transfer of equipment and materials between adjacent clean spaces

Mechanical Systems

Control airflow, filtration, temperature, and humidity based on the room’s classification and how the space is used

Our Cleanroom Process

Each MatterGuard® system is built for your specific needs

PROJECT ASSESSMENT

We review how the space is used, what is being handled, required ISO classification, pressure relationships, utilities, and the constraints that usually cause problems later if ignored.

ENGINEERING & DESIGN

The cleanroom is designed from scratch around airflow, pressure, equipment loads, cleaning regimes, and material compatibility, not around off-the-shelf layouts.

PRoject review

You receive a defined scope of work, schematic layout, technical details, timeline, and cost. These are reviewed before procurement so changes don’t surface mid-build.

FABRICATION & INSTALLATION

Panels, ceilings, interfaces, and services are manufactured and installed to the agreed tolerances, with sequencing planned to avoid rework and contamination risks.

COMMISSIONING & SUPPORT

We complete testing, documentation, and handover, then stay involved for validation support, modifications, and maintenance when the room is in use—not just when it looks finished.

Why Partner with AVM Group?

Guaranteed Room Performance

We design and build cleanroom environments that reliably perform to their required cleanliness, airflow, and pressure specifications during operation.

Customization for Every Facility Type

Each cleanroom is custom-designed to align process flow, equipment layout, utilities, and room configurations within your existing facility.

In-House Design, Fabrication & Integration

AVM Group manages the full cleanroom process in-house, from detailed design and CAD modeling through wall systems, ceilings, doors, and integration with HVAC and utilities.

Expert Support From Design to Maintenance

We support the full cleanroom lifecycle, from early planning and installation through commissioning, validation support, and long-term service.

What Our Partners Are Saying

Real results from our clients

"This new cleanroom is going to allow us to have increased production capabilities to meet our customer’s growing demands. AVM is right there with you every step of the way to make sure your requirements are fully met."

"Our operations benefit from their functionality and versatility. Additionally, employees are comfortable working in the cleanroom environment which is very important to us! "

Our Satisfied Customers include

Featured Project

Class 100 Ballroom-Style Cleanroom

We completed the construction of a Class 100 Ballroom-Style Cleanroom for a customer in the fittings industry.

Have Other Questions?

We’re happy to talk through your project needs. Give us a call today.

Cleanroom FAQS

What are ISO 14644-1 cleanroom standards?

ISO 14644-1 is the international standard that classifies cleanrooms by allowable airborne particle levels. It provides the framework used to design, test, and validate cleanrooms across industries such as pharmaceuticals, medical devices, and advanced manufacturing.

What is cleanroom integrity?

Cleanroom integrity refers to a cleanroom’s ability to maintain controlled environmental conditions, including particulate levels, airflow, and pressure differentials. Proper integrity ensures contaminants do not enter or escape the controlled space during operation or validation.

How are pressure differentials maintained in a cleanroom?

Pressure differentials are maintained through controlled HVAC systems, sealed room construction, and properly designed doors and penetrations. These elements work together to ensure air flows in the correct direction and contaminants do not migrate between spaces.

How do cleanroom wall panels and flooring systems support ISO cleanroom compliance?

Cleanroom wall panels and flooring systems create the sealed containment envelope of an ISO cleanroom. When designed as an integrated system with sealed transitions, they help control particulates, maintain pressure differentials, and support successful ISO cleanroom validation.

How does AVM Group design cleanrooms to meet validation requirements?

Our cleanrooms are designed using detailed engineering studies that account for airflow, pressure differentials, materials, and sealing methods. These designs support regulatory validation by minimizing leakage points and maintaining consistent environmental control.

Ready to Get Started?

Let our expert sales team guide you through design and budgeting for your project. You’ll receive a comprehensive and accurate quote at no cost.

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