Cleanroom Design in 10 Easy Steps

"Easy" may not be a word that comes to mind for designing such sensitive environments. However, that
doesn't mean you can't produce a solid cleanroom design by tackling issues in a logical sequence. This article
covers each key step, down to handy application-specific tips for adjusting load calculations, planning
exfiltration paths, and angling for adequate mechanical room space relative to the cleanroom's class.

Many manufacturing processes need the very stringent environmental conditions provided by a cleanroom.
Because cleanrooms have complex mechanical systems and high construction, operating, and energy costs, it
is important to perform the cleanroom design in a methodical way. This article will present a step-by-step
method for evaluating and designing cleanrooms, factoring in people/material flow, space cleanliness
classification, space pressurization, space supply airflow, space air exfiltration, space air balance, variables to
be evaluated, mechanical system selection, heating/cooling load calculations, and support space
requirements.

Step One: Evaluate Layout for People/Material Flow

It is important to evaluate the people and material flow within the cleanroom suite. Cleanroom workers are a
cleanroom's largest contamination source and all critical processes should be isolated from personnel access
doors and pathways.

The most critical spaces should have a single access to prevent the space from being a pathway to other, less
critical spaces. Some pharmaceutical and biopharmaceutical processes are susceptible to cross-contamination
from other pharmaceutical and biopharmaceutical processes. Process cross-contamination needs to be
carefully evaluated for raw material inflow routes and containment, material process isolation, and finished
product outflow routes and containment. Figure 1 is an example of a bone cement facility that has both critical
process ("Solvent Packaging", "Bone Cement Packaging") spaces with a single access and air locks as buffers
to high personnel traffic areas ("Gown", "Ungown").

Step Two: Determine Space Cleanliness Classification

To be able to select a cleanroom classification, it is important to know the primary cleanroom classification
standard and what the particulate performance requirements are for each cleanliness classification. The
Institute of Environmental Science and Technology (IEST) Standard 14644-1 provides the different cleanliness
classifications (1, 10, 100, 1,000, 10,000, and 100,000) and the allowable number of particles at different
particle sizes.
For example, a Class 100 cleanroom is allowed a maximum of 3,500 particles/cu ft and 0.1 microns and larger,
100 particles/cubic ft. at 0.5 microns and larger, and 24 particles/cubic ft. at 1.0 microns and larger. This table
provides the allowable airborne particle density per cleanliness classification table:

ISO 14644-1 Cleanroom Standards

Maximum Particles/m3
Classification FED STD
≥0.1µm ≥0.2µm ≥0.3µm ≥0.5µm ≥1µm ≥5µm
ISO 1 10 2.37 1.02 0.35 0.083 0.0029

ISO 2 100 23.7 10.2 3.5 0.83 0.029

ISO 3 1,000 237 102 35 8.3 0.029 C

ISO 4 10,000 2,370 1,020 352 83 2.9 C
ISO 5 100,000 23,700 10,200 3,520 832 29 C
ISO 6 1.0 x 106 237,000 102,000 35,200 8,320 293 Cl
ISO 7 1.0 x 107 2.37 x 106 1,020,000 352,000 83,200 2,930 Cla
ISO 8 1.0 x 108 2.37 x 107 1.02 x 107 3,520,000 832,000 29,300 Cla
ISO 9 1.0 x 109 2.37 x 108 1.02 x 108 35,200,000 8,320,000 293,000 R
Space cleanliness classification has a substantial impact on a cleanroom's construction, maintenance, and
energy cost. It is important to carefully evaluate reject/contamination rates at different cleanliness
classifications and regulatory agency requirements, such as the Food and Drug Administration (FDA).
Typically, the more sensitive the process, the more stringent cleanliness classification should be used. This
table provides cleanliness classifications for a variety of manufacturing processes:
Industrial Applications
Application Class
 Aerospace ISO C
Assembly of Touch Screen Membranes ISO
Composite Materials ISO
General Industrial ISO
Isolation of Injection Molded Parts ISO C
Optical ISO C

Electronics
Application Class
Semiconductor ISO
SMT Assembly ISO C
Solar ISO C
Wafer Board ISO

Consumables and Pharmaceuticals

Application Class
E-Liquid ISO C
Food Packaging No Cla
Nutraceutical Packaging ISO C
Pharmaceutical Compounding ISO
Pharmaceutical Packaging ISO
Sterile Compounding ISO

Medical Devices
Application Class
Device Reprocessing ISO
Inplantable Devices ISO
Medical Device Packaging ISO C
Your manufacturing process may need a more stringent cleanliness class depending upon its unique
requirements. Be careful when assigning cleanliness classifications to each space; there should be no more
than two orders of magnitude difference in cleanliness classification between connecting spaces. For example,
it is not acceptable for a Class 100,000 cleanroom to open into a Class 100 cleanroom, but it is acceptable for
a Class 100,000 cleanroom to open into a Class 1,000 cleanroom.

Looking at our bone cement packaging facility (Figure 1), "Gown", Ungown" and "Final Packaging" are less
critical spaces and have a Class 100,000 (ISO 8) cleanliness classification, "Bone Cement Airlock" and "Sterile
Airlock" open to critical spaces and have Class 10,000 (ISO 7) cleanliness classification; 'Bone Cement
Packaging" is a dusty critical process and has Class 10,000 (ISO 7) cleanliness classification, and 'Solvent
Packaging" is a very critical process and is performed in Class 100 (ISO 5) laminar flowhoods in a Class 1,000
(ISO 6) cleanroom.

Step Three: Determine Space Pressurization

Maintaining a positive air space pressure, in relation to adjoining dirtier cleanliness classification spaces, is
essential in preventing contaminants from infiltrating into a cleanroom. It is very difficult to consistently maintain
a space's cleanliness classification when it has neutral or negative space pressurization. What should the
space pressure differential be between spaces? Various studies evaluated contaminant infiltration into a
cleanroom vs. space pressure differential between the cleanroom and adjoining uncontrolled environment.
These studies found a pressure differential of 0.03 to 0.05 in w.g. to be effective in reducing contaminant
infiltration. Space pressure differentials above 0.05 in. w.g. do not provide substantially better contaminant
infiltration control then 0.05 in. w.g.

Keep in mind, a higher space pressure differential has a higher energy cost and is more difficult to control.
Also, a higher pressure differential requires more force in opening and closing doors. The recommended
maximum pressure differential across a door is 0.1 in. w.g. at 0.1 in. w.g., a 3 foot by 7 foot door requires 11
pounds of force to open and close. A cleanroom suite may need to be reconfigured to keep the static pressure
differential across doors within acceptable limits.
Our bone cement packaging facility is being built within an existing warehouse, which has a neutral space
pressure (0.0 in. w.g.). The air lock between the warehouse and "Gown/Ungown" does not have a space
cleanliness classification and will not have a designated space pressurization. "Gown/Ungown" will have a
space pressurization of 0.03 in. w.g. "Bone Cement Air Lock" and "Sterile Air Lock" will have a space
pressurization of 0.06 in. w.g. "Final Packaging" will have a space pressurization of 0.06 in. w.g. "Bone Cement
Packaging" will have a space pressurization of 0.03 in. w.g., and a lower space pressure than 'Bone Cement
Air Lock" and "Final Packaging" in order to contain the dust generated during packaging.

The air filtering into the 'Bone Cement Packaging" is coming from a space with the same cleanliness
classification. Air infiltration should not go from a dirtier cleanliness classification space to a cleaner cleanliness
classification space. "Solvent Packaging" will have a space pressurization of 0.11 in. w.g. Note, the space
pressure differential between the less critical spaces is 0.03 in. w.g. and the space differential between the
very critical "Solvent Packaging" and "Sterile Air Lock" is 0.05 in. w.g. The 0.11 in. w.g. space pressure will not
require special structural reinforcements for walls or ceilings. Space pressures above 0.5 in. w.g. should be
evaluated for potentially needing additional structural reinforcement.

Step Four: Determine Space Supply Airflow

The space cleanliness classification is the primary variable in determining a cleanroom's supply airflow.
Looking at table 3, each clean classification has an air change rate. For example, a Class 100,000 cleanroom
has a 15 to 30 ach range. The cleanroom's air change rate should take the anticipated activity within the
cleanroom into account. A Class 100,000 (ISO 8) cleanroom having a low occupancy rate, low particle
generating process, and positive space pressurization in relation to adjacent dirtier cleanliness spaces might
use 15 ach, while the same cleanroom having high occupancy, frequent in/out traffic, high particle generating
process, or neutral space pressurization will probably need 30 ach.

The designer needs to evaluate his specific application and determine the air change rate to be used. Other
variables affecting space supply airflow are process exhaust airflows, air infiltrating in through doors/openings,
and air exfiltrating out through doors/openings. IEST has published recommended air change rates in Standard
14644-4.

Looking at Figure 1, "Gown/Ungown" had the most in/out travel but is not a process critical space, resulting in
20 a ch., 'Sterile Air Lock" and "Bone Cement Packaging Air Lock" are adjacent to critical production spaces
and in the case of the "Bone Cement Packaging Air Lock", the air flows from the air lock into the packaging
space. Though these air locks have limited in/out travel and no particulate generating processes, their critical
importance as a buffer between "Gown/Ungown" and manufacturing processes results in their having 40 ach.

"Final Packaging" places the bone cement/solvent bags into a secondary package which is not critical and
results in a 20 ach rate. "Bone Cement Packaging" is a critical process and has a 40 ach rate. 'Solvent
Packaging" is a very critical process which performed in Class 100 (ISO 5) laminar flow hoods within a Class
1,000 (ISO 6) cleanroom. 'Solvent Packaging" has very limited in/out travel and low process particulate
generation, resulting in a 150 ach rate.

Cleanroom Classification and Air Changes Per Hour

Air cleanliness is achieved by passing the air through HEPA filters. The more often the air passes through the
HEPA filters, the fewer particles are left in the room air. The volume of air filtered in one hour divided by the
volume of the room gives the number of air changes per hour.

Required air changes per hour (ACH)

ISO Class Average number of air changes per hour
ISO 5 240–360 air changes per hour (unidirectional airflow)
ISO 6 90–180 air changes per hour
ISO 7 30–60 air changes per hour
ISO 8 10–25 air changes per hour
Conventional building 2–4 air changes per hour
The above-suggested air changes per hour are only a design rule of thumb. They should be computed by an
HVAC cleanroom expert, as many aspects must be taken into consideration, such as the size of the room, the
number of people in the room, the equipment in the room, the processes involved, the heat gain, etc.

Step Five: Determine Space Air Exfiltration Flow

The majority of cleanrooms are under positive pressure, resulting in planned air exfiltrating into adjoining
spaces having lower static pressure and unplanned air exfiltration through electrical outlets, light fixtures,
window frames, door frames, wall/floor interface, wall/ceiling interface, and access doors. It is important to
understand rooms are not hermetically sealed and do have leakage. A well-sealed cleanroom will have a 1% to
2% volume leakage rate. Is this leakage bad? Not necessarily.

First, it is impossible to have zero leakage. Second, if using active supply, return, and exhaust air control
devices, there needs to be a minimum of 10% difference between supply and return airflow to statically
decouple the supply, return, and exhaust air valves from each other. The amount of air exfiltrating through
doors is dependent upon the door size, the pressure differential across the door, and how well the door is
sealed (gaskets, door drops, closure).
 We know the planned infiltration/exfiltration air goes from one space to the other space. Where does the
unplanned exfiltration go? The air relieves within the stud space and out the top. Looking at our example
project (Figure 1), the air exfiltration through the 3- by 7- foot door is 190 cfm with a differential static pressure
of 0.03 in w.g. and 270 cfm with a differential static pressure of 0.05 in. w.g.

Step Six: Determine Space Air Balance

Space air balance consists of adding all the airflow into the space (supply, infiltration) and all the airflow leaving
the space (exhaust, exfiltration, return) being equal. Looking at the bone cement facility space air balance
(Figure 2), "Solvent Packaging" has 2,250 cfm supply airflow and 270 cfm of air exfiltration to the 'Sterile Air
Lock", resulting in a return airflow of 1,980 cfm. "Sterile Air Lock" has 290 cfm of supply air, 270 cfm of
infiltration from 'Solvent Packaging", and 190 cfm exfiltration to "Gown/Ungown", resulting in a return airflow of
370 cfm.

"Bone Cement Packaging" has 600 cfm supply airflow, 190 cfm of air filtration from 'Bone Cement Air Lock",
300 cfm dust collection exhaust, and 490 cfm of return air. "Bone Cement Air Lock" has 380 cfm supply air,
190 cfm exfiltration to 'Bone Cement Packaging" has 670 cfm supply air, 190 cfm exfiltration to
"Gown/Ungown". "Final Packaging" has 670 cfm supply air, 190 cfm exfiltration to 'Gown/Ungown", and 480
cfm of return air. "Gown/Ungown" has 480 cfm of supply air, 570 cfm of infiltration, 190 cfm of exfiltration, and
860 cfm of return air.

We have now determined the cleanroom supply, infiltration, exfiltration, exhaust, and return airflows. The final
space return airflow will be adjusted during start-up for unplanned air exfiltration.

Step Seven: Assess Remaining Variables

Other variables needing to be evaluated include:

 Temperature: Cleanroom workers wear smocks or full bunny suits over their regular clothes to reduce
particulate generation and potential contamination. Because of their extra clothing, it is important to maintain a
lower space temperature for worker comfort. A space temperature range between 66°F and 70° will provide
comfortable conditions.
 Humidity: Due to a cleanroom's high airflow, a large electrostatic charge is developed. When the ceiling and
walls have a high electrostatic charge and space has a low relative humidity, airborne particulate will attach
itself to the surface. When the space relative humidity increases, the electrostatic charge is discharged and all
the captured particulate is released in a short time period, causing the cleanroom to go out of specification.
Having high electrostatic charge can also damage electrostatic discharge sensitive materials. It is important to
keep the space relative humidity high enough to reduce the electrostatic charge build-up. An RH or 45% +5%
is considered the optimal humidity level.
 Laminarity: Very critical processes might require laminar flow to reduce the chance of contaminates getting into
the air stream between the HEPA filter and the process. IEST Standard #IEST-WG-CC006 provides airflow
laminarity requirements.
 Electrostatic Discharge: Beyond the space humidification, some processes are very sensitive to electrostatic
discharge damage and it is necessary to install grounded conductive flooring.
 Noise Levels and Vibration: Some precision processes are very sensitive to noise and vibration.
Step Eight: Determine Mechanical System Layout
A number of variables affect a cleanroom's mechanical system layout: space availability, available funding,
process requirements, cleanliness classification, required reliability, energy cost, building codes, and local
climate. Unlike normal A/C systems, cleanroom A/C systems have substantially more supply air than needed
to meet cooling and heating loads.

Class 100,000 (ISO 8) and lower ach Class 10,000 (ISO 7) cleanrooms can have all the air go through the
AHU. Looking at Figure 3, the return air and outside air are mixed, filtered, cooled, reheated, and humidified
before being supplied to terminal HEPA filters in the ceiling. To prevent contaminant recirculation in the
cleanroom, the return air is picked up by low wall returns. For higher class 10,000 (ISO 7) and cleaner
cleanrooms, the airflows are too high for all the air to go through the AHU. Looking at Figure 4, a small portion
of the return air is sent back to the AHU for conditioning. The remaining air is returned to the circulation fan.

Alternatives to Traditional Air Handling Units

 Fan filter units, also known as integrated blower modules, are a modular cleanroom filtration solution with
some advantages over traditional air handling systems. They are applied in both small and large spaces with a
cleanliness rating as low as ISO Class 3. Air change rates and cleanliness requirements determine the number
of fan filters required. An ISO Class 8 cleanroom ceiling may only require 5-15% of ceiling coverage while an
ISO Class 3 or cleaner cleanroom may require 60-100% coverage.

Find Out if Your Facility would Benefit from a Modular Fan Filter System over a Traditional Air Handling Unit
Step Nine: Perform Heating/Cooling Calculations
When performing the cleanroom heating/cooling calculations, take the following into consideration:

 Use the most conservative climate conditions (99.6% heating design, 0.4% drybulb/median wetbulb cooling
deign, and 0.4% wetbulb/median drybulb cooling design data).
 Include filtration into calculations.
 Include humidifier manifold heat into calculations.
 Include process load into calculations.
 Include recirculation fan heat into calculations.
Step Ten: Fight for Mechanical Room Space
Cleanrooms are mechanically and electrically intensive. As the cleanroom's cleanliness classification becomes
cleaner, more mechanical infrastructure space is needed to provide adequate support to the cleanroom. Using
a 1,000-sq-ft cleanroom as an example, a Class 100,000 (ISO 8) cleanroom will need 250 to 400 sq ft of
support space, a Class 10,000 (ISO 7) cleanroom will need 250 to 750 sq ft of support space, a Class 1,000
(ISO 6) cleanroom will need 500 to 1,000 sq ft of support space, and a Class 100 (ISO 5) cleanroom will need
750 to 1,500 sq ft of support space.

The actual support square footage will vary depending upon the AHU airflow and complexity (Simple: filter,
heating coil, cooling coil, and fan; Complex: sound attenuator, return fan, relief air section, outside air intake,
filter section, heating section, cooling section, humidifier, supply fan, and discharge plenum) and number of
dedicated cleanroom support systems (exhaust, recirculation air units, chilled water, hot water, steam, and
DI/RO water). It is important to communicate the required mechanical equipment space square footage to the
project architect early in the design process.

Final Thoughts
Cleanrooms are like race cars. When properly designed and built, they are highly efficient performance
machines. When poorly designed and built, they operate poorly and are unreliable. Cleanrooms have many
potential pitfalls, and supervision by an engineer with extensive cleanroom experience is recommended for
your first couple of cleanroom projects