- A cleanroom is a modular environment in which the following environmental factors are kept under control, temperature, airborne particulates, microbes, relative humidity, differential pressure, and air flow.
- Cleanroom Validation is performed for a variety of reasons. To ensure that the design of the facility is fit for its intended purpose; to ensure that the facility, equipment, and environment meet User Requirement Specifications (URS); to ensure that the facility, equipment, and environment meet defined regulatory requirements; to ensure that the facility, equipment, and its environment function together as a system to meet defined standards.
- Cleanrooms are validated and then certified to a chosen class of ISO 14644-1. Each class of ISO14544-1 has its unique requirements that must be made for a facility to be classified in the specified classification.
CLEANROOM VALIDATION LIFE CYCLE
Validation of a new cleanroom follows a specified lifecycle. The life cycle comprises five phases each of which accomplishes particular tasks to control variation in the modular environment.
Cleanroom validation work is accomplished through five phases. It starts off with the design control phase and ends with monitor and control. Changes to equipment and control factors after the cleanroom has been validated are grounds for cleanroom re-validation.
Phase 1: Design Qualification
Cleanroom validation starts with Design Qualification (DQ). The purpose of this phase is to prove through objective evidence that the design is fit for its intended purpose. Design Qualification is a verification exercise against requirements defined in the acceptance criteria of your DQ protocol.
The protocol should address the following:
- User Requirement Specifications (URS)
- Vendor documents and specifications
- Facility layout
- Purchase orders
- Design documentation
- Factory Acceptance Tests (FATs)
- As-built drawings.
- Datasheets
The output of the Design Qualification phase is a phase report and a Standard Documentation List (SDL) file that documents the following:
- Design requirements
- Bidding requirements
- Purchasing and order documentation
- Vendor-supplied documents list.
- As-built drawings.
- Component lists
- Inspection lists
- Factory Acceptance Tests
The approval of the Design Qualification, DQ phase is a pre-requisite for the initiation of the Installation Qualification, IQ phase.
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Phase 2: Installation Qualification
The purpose of this Installation Qualification (IQ) phase is to confirm through verification that the equipment as installed confirms user requirements and design requirements.
Verification is focused on the following items that should be called for in your IQ protocol:
- HVAC calibration
- P&ID loop verification
- HEPA filter integrity test data review
- Critical equipment calibration status
- Site Acceptance Tests (SATs)
- Installation Qualification tests
- Piping and welding documentation
- Utility verification
- System standard operating procedures and work instructions
The output of this phase should be an IQ report addressing all the above elements, and an SDL file that documents the following elements:
- Project changes
- IQ tests were performed.
- Calibration
- Supplier-supplied documents.
- Equipment certificate
- Installation deviations
- Site Acceptance Tests (SAT)
- Consumable list
- Spare part list
- Environmental review report
- List of Operational and Instructional documents
IQ approval is a pre-requisite for the start of the Operational Qualification (OQ) phase.
Phase 3: Operation Qualification
The objective for this Operational Qualification (OQ) phase is to show through objective evidence that the cleanroom operates in conformance with design requirements and user-defined requirements, and that it consistently operates within a defined range of conditions.
The OQ protocol should address the following:
- Testing HVAC (Heating - Ventilation - Air Conditioner) system operation against specified functional requirements
- Critical Alarms
- Interlock Alarms
- Critical operating parameters are defined on the room data sheet.
- Filter integrity tests
- The standard operation for the cleanroom
- Airspeed and airflow
- Airflow patterns
- Pressure differential
The OQ phase should also address worst-case scenarios. To design the worst-case scenario for the operation of the cleanroom, critical operating parameters are identified from the cleanroom data sheet. Operation ranges, and extreme ranges, are set for each critical parameter and a worst-case is designed and documented. It should include the following:
- Maximum and minimum temperatures
- Maximum and minimum humidity
- Maintenance schedules
- Personnel contamination
The worst-case scenario is usually carried out at the specified High and specified Low parameters.
The output of this phase is an OQ report addressing alarms and functional requirements of the cleanroom specified in the user requirement specifications.
Phase 4: Performance Qualification
The purpose of the Performance Qualification (PQ) of the cleanroom is to demonstrate with objective evidence that the cleanroom consistently operates within defined parameters to produce the defined, desired environmental outcome.
Cleanroom performance qualification involves testing and monitoring of the following:
- Airborne particulate levels
- Surface particulate levels
- Viable microbial particulates
- Relative humidity
- Differential pressure
- Temperature
The output of the PQ phase is a PQ report that analyzes the performance of the cleanroom using specified equipment parameters. PQ is a pre-requisite for certification.
CLEANROOM CERTIFICATION
Validated cleanrooms are validated to a required class of cleanliness. The level of cleanliness chosen is driven by user requirements. Cleanroom classes are defined in ISO1464-1:
Methods for evaluation and measurements for Certification are specified in ISO14644-3. It calls out for the following ten tests.
- Airborne particle count test
- Airflow test
- Air pressure differential test
- Filter leakage test
- Flow visualization test
- Airflow direction test
- Temperature test
- Humidity test
- Recovery test
- Containment leak test
Once certified to a particular class the cleanroom factors are monitored to ensure that parameters have not drifted, or changed and that the environment is under control.
Phase 5: Control and Monitor
A constant monitoring program is required after certification. Requirements for compliance are found in ISO 14644-2.
Statistical analysis for cleanroom parameters is encouraged as a tool for monitoring the cleanroom after certification to ensure compliance. The tool of choice is statistical process control, SPC.
