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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? *

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