Short answer

Cleanroom panels are prefabricated sandwich panels, typically 50–100 mm (2–4 in) thick and 950–1200 mm wide, with 0.5–0.6 mm coated-steel or stainless skins over rock wool, honeycomb, magnesium-oxide or PU/PIR cores. They form airtight, flush, cleanable walls and ceilings for rooms classified ISO 5 to ISO 8 under ISO 14644-1 or GMP grades A to D.

Key takeaways

  • ISO 14644-1 class ISO 5 allows 3,520 particles of 0.5 µm or larger per m³; each class above allows ten times more.
  • Cleanroom wall panels are typically 50 mm thick for partitions and 75–100 mm for insulated or perimeter walls.
  • Rock wool cores suit fire-critical pharma rooms; PU/PIR cores (about 0.022 W/(m·K)) suit temperature-controlled and cold GMP rooms.
  • Pressure differences between adjacent cleanroom grades are commonly 10–15 Pa, so walls and penetrations must be nearly airtight.
  • Coved corners of about 50 mm radius, flush windows and flush doors remove ledges where particles collect.
  • Pharmaceutical cold rooms at +2 °C to +8 °C typically use 100 mm (4 in) PU/PIR panels and must be temperature-mapped before use.

What are cleanroom panels?

Cleanroom panels are prefabricated sandwich panels, typically 50–100 mm (2–4 in) thick, with smooth coated-steel, stainless or aluminium skins over a rock wool, honeycomb, magnesium-oxide or PU/PIR core, used to build the walls and ceilings of controlled-environment rooms. Their faces shed no particles, resist cleaning chemicals and join flush, so the room can be held at a specified particle class and pressure.

A cleanroom is a room in which airborne particles are controlled to a defined level, set out in ISO 14644-1. The HVAC system and HEPA filters do the cleaning; the panels make that possible by giving an airtight, smooth, cleanable shell with no ledges, gaps or porous surfaces where particles and microbes can collect. Pharmaceutical plants, hospitals, electronics and semiconductor fabs, laboratories, food and cosmetics factories all use them.

This guide covers cleanroom classes, panel cores and facings, the details that separate a cleanroom wall system from an ordinary partition, modular and prefabricated cleanrooms, and the special case of temperature-controlled GMP rooms in the pharmaceutical cold chain.

Cleanroom classes: ISO 14644-1 and EU GMP grades

ISO 14644-1 classifies cleanrooms from ISO 1 (cleanest) to ISO 9 by the maximum number of particles per cubic metre of air; ISO 5 allows 3,520 particles of 0.5 µm or larger per m³, and each step up allows ten times more. EU GMP Annex 1 grades pharmaceutical rooms A to D, which map onto ISO classes.

ISO classMax particles ≥ 0.5 µm per m³EU GMP grade (approx.)Typical air changes per hourTypical uses
ISO 53,520Grade A; Grade B at restUnidirectional flow, about 0.36–0.54 m/s (70–105 ft/min)Aseptic filling, critical zones
ISO 635,200—About 90–180Electronics assembly, some device work
ISO 7352,000Grade B in operation; Grade C at restAbout 30–60Pharmaceutical background rooms, compounding
ISO 83,520,000Grade C in operation; Grade D at restAbout 10–25Packaging, gowning, medical devices, food
ISO 935,200,000—Room airOrdinary controlled rooms

Air change rates are typical design ranges, not requirements; the real number comes from the particle load, room size and process. Pressure cascades between adjacent grades are commonly 10–15 Pa (0.04–0.06 in wg), from cleanest to least clean, which means the walls, ceiling, doors and penetrations must be close to airtight.

What is the best cleanroom wall material?

The best cleanroom wall material is a smooth, non-shedding, chemically resistant panel face, usually pre-painted galvanised steel of 0.5–0.6 mm for most rooms and 304 stainless for wet, aggressive or high-grade zones, over a core chosen for fire, strength and insulation. Ordinary painted plasterboard sheds dust, absorbs moisture and cracks at joints, so it is avoided in classified rooms. Our hygienic wall panels guide compares FRP, PVC and stainless linings for less critical food areas.

Panel cores

CoreFire behaviourInsulationWeight / strengthBest for
Rock woolNon-combustible core; panels commonly A2-s1,d0 with fire ratings availableAbout 0.040 W/(m·K)Heavier, good rigidityPharma and hospital cleanrooms where fire rules are strict
Paper honeycombCombustible, limitedPoorLight, very flatElectronics, low-cost ISO 7–8 rooms
Aluminium honeycombNon-combustible corePoorLight, very stiff, flatHigh-grade rooms, walkable ceilings
Magnesium oxide / glass-magnesium boardNon-combustible coreLowHeavy, hardImpact-prone walls, fire zones
PU / PIR foamPIR better than PU; check classBest: about 0.022 W/(m·K)Light, strongTemperature-controlled cleanrooms, cold GMP rooms, food plants

Insulation matters more than many buyers expect. A cleanroom held at 20 ± 2 °C (68 ± 4 °F) and 45 ± 5% RH next to a hot plant room, or a 2–8 °C cleanroom, needs insulated walls to stop condensation and keep HVAC loads down. For cold rooms, PU/PIR cores are the standard; our rock wool sandwich panels guide covers fire-rated cores in more detail.

Panel facings and coatings

  • Polyester (PE) coated steel: standard for ISO 7–8 rooms and food.
  • PVDF coated steel: better chemical and UV resistance.
  • Antistatic coatings: for electronics, where surface charges attract particles and damage components.
  • Antibacterial coatings: hospitals and some pharma areas, though cleaning regime matters more than coating.
  • Stainless steel 304 / 316: wet areas, aggressive disinfectants such as hydrogen peroxide vapour or chlorine, and highest-grade zones.

Always check the facing against the actual disinfectants used, including sporicides and vaporised hydrogen peroxide, and their concentrations.

What makes a cleanroom wall system different from a normal partition?

A cleanroom wall system differs from an ordinary partition in its flush details: every window, door, light, socket and return-air grille sits flush with the panel face, all internal corners are coved, joints are sealed airtight, and nothing projects to collect dust.

  • Coved corners: aluminium or PVC coving of about 50 mm (2 in) radius at wall-wall, wall-ceiling and wall-floor junctions so surfaces can be wiped in one pass.
  • Flush windows: double-glazed, sealed, set flush on both faces, often with a dry desiccant between panes.
  • Flush doors: steel or stainless doors with drop-down seals, interlocks for airlocks, and vision panels.
  • Panel joints: tongue-and-groove or aluminium-profile joints sealed with cleanroom-grade silicone, sometimes hidden behind a flush H-section.
  • Return-air walls: double-skin walls with low-level grilles that carry air back to the air handler.
  • Ceilings: walkable ceiling panels for maintenance access, with flush openings for HEPA filter housings and fan filter units, and sealed light fittings.
  • Services: conduits and pipework run inside the panel core or through sealed, flush penetrations.

Airtightness is tested: rooms are typically pressure-tested and particle-counted during qualification, so a small unsealed gap at a light fitting can cause a room to fail. That is why panels and their accessories should come from one system.

Modular cleanroom and prefabricated cleanroom systems

A modular cleanroom is built from factory-made panels, ceilings, doors, windows and HVAC components assembled on site, rather than from site-built stud walls and plaster. Modular systems go up faster, are cleaner to install, and can be extended, relocated or reconfigured later.

TypeConstructionTypical classesProsCons
Hardwall modular (sandwich panel)50–100 mm panels on a floor track, walkable or suspended ceilingISO 5–8, GMP B–DDurable, airtight, pressure-capable, insulated optionsHigher cost than softwall
SoftwallSteel frame with vinyl curtains and fan filter unitsISO 7–8Low cost, fast, movableWeak pressure control, not for GMP
Rigid-wall (acrylic or polycarbonate)Frame with clear rigid panelsISO 5–8Visibility, modest costLess airtight, limited size
Prefab containerised or podComplete factory-built room shipped as a unitISO 5–8Shortest site time, pre-testedTransport size limits

For pharmaceutical GMP work, hardwall sandwich panel systems are the norm because they can hold pressure cascades and withstand repeated disinfection. Prefabricated cleanroom panels are usually 950–1200 mm wide and cut to room height, typically up to 3–4 m for walls.

Cold chain GMP: temperature-controlled cleanrooms and cold rooms

In the pharmaceutical cold chain, GMP and GDP rules require medicines to be stored and handled within their labelled temperature range, most often +2 °C to +8 °C (36–46 °F), with the room mapped and continuously monitored. Cold rooms for this purpose are built from PU/PIR sandwich panels, and some processing rooms combine cleanroom class with refrigeration.

  • Panels: 100 mm (4 in) PU/PIR for +2 °C to +8 °C rooms and 150–200 mm (6–8 in) for −20 °C storage, with hygienic coated or stainless faces and sealed joints; see the cold room panel thickness guide.
  • Mapping: EU GDP guidelines (2013/C 343/01) require temperature mapping of storage areas before use; see our warehouse temperature mapping guide.
  • GMP temperature monitoring: a GMP temperature monitoring system uses calibrated sensors, continuous logging with an audit trail and alarms; see cold room temperature monitoring.
  • Redundancy: duplicate refrigeration and backup power are common for high-value stock.

Our pharmaceutical cold chain and vaccine storage guide covers the 2–8 °C rules, equipment and validation in detail.

How cleanroom panels are installed

Cleanroom panels are installed after the building is weathertight and the floor is level, starting with floor tracks and ending with sealing and cleaning, so that construction dust does not end up inside the finished room.

  1. Set out the layout on a level floor; tolerance is usually within a few millimetres over the room length.
  2. Fix floor and ceiling tracks or support structure, with the ceiling suspension designed for walkable panels if specified.
  3. Erect wall panels in sequence, with conduits and services pre-installed in the cores where required.
  4. Install ceiling panels, filter housings, lights and access hatches.
  5. Fit doors, windows, pass boxes and air showers flush with the walls.
  6. Fit coving at every internal corner and the wall-floor junction, then lay the seamless floor (vinyl or epoxy) up to the coving.
  7. Seal all joints with cleanroom-grade silicone.
  8. Clean from top to bottom, then commission HVAC and carry out pressure, airflow and particle-count testing to ISO 14644.

Cleanroom panel specification: typical values

Typical clean room wall panels are 50 mm (2 in) thick for internal partitions and 75–100 mm (3–4 in) for insulated or perimeter walls, about 950–1200 mm wide, with 0.5–0.6 mm coated-steel skins.

  • Thickness: 50 mm standard; 75–100 mm where insulation, acoustic or fire performance is needed; 100–200 mm for cold rooms.
  • Width: about 950–1200 mm.
  • Skins: 0.5–0.6 mm coated steel, 0.6–0.8 mm stainless, or aluminium.
  • Flatness: panels must be flat enough that light reflections do not show waviness, which also shows where dust lands.
  • Fire: confirm classification and fire resistance against local codes for the room's use.

How to choose cleanroom panels: checklist

Choose cleanroom panels by class, process, fire rules, temperature and the disinfectants you will use.

  • Class: confirm the ISO class or GMP grade for each room and the pressure cascade.
  • Fire: rock wool or other non-combustible cores where codes or insurers require them.
  • Temperature: PU/PIR insulated panels for cold rooms and rooms with tight temperature control.
  • Chemicals: facings compatible with your disinfectants; stainless for the most aggressive.
  • Details: flush windows, doors and fittings, coved corners and walkable ceilings from one system.
  • Validation: documentation for materials, airtightness and qualification testing.

Be There supplies PU and PIR insulated sandwich panels with coated steel, stainless or aluminium facings, 50–200 mm thick and up to 12 m long, used for hygienic and temperature-controlled rooms, as well as complete walk-in cold room kits for +2 °C to +8 °C pharmaceutical and food storage. We do not supply HEPA filtration, cleanroom HVAC or validation services, so your cleanroom contractor will specify those. Send your room layout, class, temperature and facing requirements through the inquiry form and we will quote FOB, CIF or DDP.

Quick answers

What are cleanroom walls made of?
Cleanroom walls are usually made of prefabricated sandwich panels with smooth pre-painted galvanised steel or stainless steel skins about 0.5–0.8 mm thick, bonded to a core of rock wool, paper or aluminium honeycomb, magnesium oxide board or PU/PIR foam. They are joined with sealed, flush joints and coved corners so the surface does not shed or trap particles.
How much does a modular cleanroom cost?
Modular cleanroom cost varies widely with class, size, HVAC and validation. As a broad indication, a simple softwall ISO 8 room can cost a few hundred US dollars per m², while hardwall ISO 7 or GMP rooms with HVAC, HEPA filtration and qualification often run from about US$1,000 to several thousand per m². Panels are typically a minority of the total.
What is the difference between hardwall and softwall cleanrooms?
A hardwall cleanroom uses rigid sandwich panels for walls and ceiling, holds positive pressure well and withstands repeated disinfection, so it is used for pharmaceutical GMP and higher classes. A softwall cleanroom uses vinyl curtains on a steel frame with fan filter units. It is cheaper and portable but has weak pressure control and suits ISO 7–8 work.
Can PU or PIR panels be used in cleanrooms?
Yes, PU and PIR sandwich panels are used for cleanrooms that need insulation, such as temperature-controlled production rooms, cold GMP rooms and food plants, because their foam core gives about 0.022 W/(m·K). Where local fire codes or insurers require non-combustible cores, rock wool or magnesium-oxide panels are specified instead, sometimes alongside PIR in cold zones.
What is a GMP temperature monitoring system?
A GMP temperature monitoring system continuously records the temperature, and often humidity, of pharmaceutical storage and production areas using calibrated sensors, secure data logging with an audit trail, and alarms by SMS, email or call when limits are exceeded. Systems used for GMP records are typically expected to meet data-integrity requirements such as 21 CFR Part 11 or EU GMP Annex 11.
How thick are cleanroom panels?
Most cleanroom wall panels are 50 mm (2 in) thick, which gives enough stiffness for partitions up to about 3–4 m high and room for conduits in the core. Perimeter walls, fire-rated walls and insulated rooms use 75–100 mm (3–4 in), and cold rooms inside pharmaceutical facilities use 100–200 mm PU/PIR depending on temperature.