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Life-Sciences eQMS 13 items

HVAC and Cleanroom Qualification Checklist

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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