CYTOTOXIC CABINET TESTING

NATA Accredited Cytotoxic Drug Safety Cabinet (CDSC) Testing

Airepure NATA certified technicians are accredited to perform various compliance tests to validate cytotoxic drug safety cabinets, as per the following Australian and International Standards:

  • AS 1807.1 – Determination of air velocity and uniformity in clean work stations, laminar flow safety cabinets and pharmaceutical isolators
  • AS 1807.5 – Determination of work zone integrity
  • AS 1807.6 – Determination of integrity for terminally mounted HEPA Filter installations.
  • AS 1807.15 – Determination of illuminance
  • AS 1807.20 – Determination of sound level at installed work stations, safety cabinets and pharmaceutical isolators
  • AS 1807.21 – Determination of inward air velocity
  • AS 1807.22 – Determination of air barrier containment of laminar flow safety cabinets
  • NSF/ANSI 49 Biosafety Cabinetry Certification (Annex F.2) Downflow Velocity
  • NSF/ANSI 49 Biosafety Cabinetry Certification (Annex F.3) Inflow Velocity (face velocity) test
  • NSF/ANSI 49 Biosafety Cabinetry Certification (Annex F.5) HEPA Filter Leak Test
  • NSF/ANSI 49 Biosafety Cabinetry Certification (Annex F.7) Site installation assessment tests
  • NSF/ANSI 49 Biosafety Cabinetry Certification (Annex F.9) Lighting intensity test
  • NSF/ANSI 49 Biosafety Cabinetry Certification (Annex F.11) Noise level test

At the conclusion of our comprehensive testing, you will receive a detailed analysis report and a NATA endorsed Certificate of Compliance to verify that your cytotoxic drug safety cabinet meets Australian and International Standard specifications.

Pharmaceutical Isolator Testing

Airepure NATA certified technicians are accredited to perform various compliance tests to validate pharmaceutical isolators, as per the following Australian and International Standards:

  • AS 1807.1 – Determination of air velocity and uniformity in clean work stations, laminar flow safety cabinets and pharmaceutical isolators
  • AS 1807.5 – Determination of work zone integrity
  • AS 1807.6 – Determination of integrity for terminally mounted HEPA Filter installations.
  • AS 1807.15 – Determination of illuminance
  • AS 1807.20 – Determination of sound level at installed work stations, safety cabinets and pharmaceutical isolators
  • AS 1807.21 – Determination of inward air velocity
  • AS 1807.22 – Determination of air barrier containment of laminar flow safety cabinets
  • NSF/ANSI 49 Biosafety Cabinetry Certification (Annex F.2) Downflow Velocity
  • NSF/ANSI 49 Biosafety Cabinetry Certification (Annex F.3) Inflow Velocity (face velocity) test
  • NSF/ANSI 49 Biosafety Cabinetry Certification (Annex F.5) HEPA Filter Leak Test
  • NSF/ANSI 49 Biosafety Cabinetry Certification (Annex F.7) Site installation assessment tests
  • NSF/ANSI 49 Biosafety Cabinetry Certification (Annex F.9) Lighting intensity test
  • NSF/ANSI 49 Biosafety Cabinetry Certification (Annex F.11) Noise level test

At the conclusion of our comprehensive testing, you will receive a detailed analysis report and a NATA endorsed Certificate of Compliance to verify that your pharmaceutical isolator meets Australian and International Standard specifications.

When should Cytotoxic Cabinets be tested?

  • On site, prior to use, upon installation and/or commissioning.
  • After any mechanical or electrical maintenance.
  • After filter replacement.
  • After re-location of clean work stations or safety cabinets.
  • Re-tested at least annually
  • Re-tested as required by appropriate regulatory authority.
  • In special circumstances, such as a significant change in the work program, or where impaired operation is suspected.

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