생명과학 eQMS 13개 항목
HVAC and Cleanroom Qualification Checklist
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Verifies that HVAC systems and classified cleanrooms are qualified for air classification, pressure cascade, recovery, and environmental control in sterile and non-sterile manufacturing. Use to plan or audit cleanroom qualification.
EU GMP Annex 1ISO 14644-1ISO 14644-221 CFR 211.46
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Design and Classification
Confirm the design basis and grade.
- Is each room assigned an air cleanliness grade (A/B/C/D) or ISO class appropriate to the operations performed? *
- Is airborne particle classification performed at rest and in operation per ISO 14644-1? *
- Are HEPA filters installed, tested for integrity, and leak-tested in place? *
- Record the design air change rate per hour for the critical area.
Pressure Cascade and Airflow
- Is a documented pressure cascade maintained between adjacent rooms of differing grades (typically 10-15 Pa)? *
- Are airflow visualization (smoke) studies performed for Grade A and unidirectional flow zones? *
- Is air velocity at the working position verified for unidirectional airflow? *
- Are room recovery times measured to confirm restoration of classification? *
Environmental Parameters
- Are temperature and relative humidity controlled and verified against defined limits? *
- Is microbial monitoring (settle plates, active air, surface) integrated with qualification? *
Requalification and Monitoring
- Is periodic requalification scheduled per the required frequency for each grade? *
- Is a continuous monitoring program in place for Grade A and Grade B viable and non-viable particles? *
- Are HVAC changes managed through change control with impact assessment on classification? *
HVAC and Cleanroom Qualification Checklist 체크리스트 전체 다운로드
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