Camfil is an IANZ accredited organisation that complies with the requirements of NZ ISO/IEC 17025:2017 for general requirements for the competence of testing and calibration laboratories.
We provide professional, on-site IANZ accredited testing and certification services to help organisations meet and maintain International and Australian standards for controlled environments, and ensure the conformance, ongoing safety and operating efficiency of contamination control equipment.
Our services include IANZ testing and compliance certification for controlled environments, and HEPA filter supply and replacement. These include hospital cleanrooms, pharmaceutical cleanrooms, manufacturing cleanrooms, biological safety cabinets, fume cabinets/cupboards, cytotoxic drug safety cabinets, clean work stations, pharmaceutical isolators, laminar air flow systems and airborne containment systems.
We are also accredited for biological conditions (air impaction methods) testing for yeast, mould and bacteria. We test spray booths and have registered IQP’s (independent qualified person) to generate and sign 12A forms for spray booths and ducted fume cabinets for the purpose of building BWOF.
Out of our scope of accreditation we test compressed air for dew point, microbial, air quality and oil content in manufacturing environments.
ON-SITE MECHANICAL TESTING SERVICES
Our IANZ certification services are provided on-site and are scheduled for your convenience. They include:
- HEPA filter testing
- Cleanroom certification
- Clean workstation testing
- Biosafety cabinet certification
- Fume cupboard testing
- Cytotoxic cabinet testing
- Safety cabinet fumigation
- Compressed air testing
- Microbial testing
SCOPE OF ON-SITE MECHANICAL TESTING SERVICES
Our IANZ accredited facilities comply with the requirements of NZ ISO/IEC 17025:2017.
We are able to provide professional on-site equipment and facility testing in accordance with the following methods, or in accordance with standards or specifications using technically equivalent test methodology:
Controlled Environments 6.95
By the methods of:
- AS1386.5 – Cleanrooms and clean workstations – Clean workstations
- AS1807.0 – Apparatus
- AS 1807.1 – Determination of air flow and uniformity of air velocity in clean work stations and laminar flow safety cabinets
- AS 1807.3 – Determination of air velocity and uniformity of air velocity in laminar flow clean rooms
- AS 1807.5 – Determination of work zone integrity
- AS 1807.6 – Determination of integrity of terminally mounted HEPA filter installations
- AS 1807.7 – Determination of integrity of HEPA filter installations not terminally mounted
- AS 1807.8 – Particle counting in work zone by automatic particle counter
- AS 1807.10 – Determination of air pressure of cleanrooms
- AS 1807.11 – Determination of airflow parallelism in laminar flow cleanrooms
- AS 1807.12 – Determination of temperature in work zones
- AS 1807.13 – Determination of relative humidity in cleanrooms
- AS 1807.15 – Determination of illuminance
- AS 1807.16 – Determination of sound level in cleanrooms
- AS 1807.20 – Determination of sound level at installed workstations and safety cabinets
- AS 1807.21 – Determination of inward air velocity of Class I biological safety cabinets
- AS 1807.22 – Determination of air barrier containment of laminar flow safety cabinets
- AS 1807.23 – Determination of intensity of radiation from germicidal ultraviolet lamps
- AS 1807.24 – Determination of recovery times of cleanrooms
- AS 2107 – Acoustics – recommended design sound levels and reverberation times for building interiors
- AS/NZS 2243.8 – Safety in laboratories – fume cabinets
- AS 2243.9 – Safety in laboratories – recirculating fume cabinets
- AS 2252.1 – Biological safety cabinets (Class I) for personnel and environmental protection; clauses 5.1.5 and 5.1.6 only
- AS 2252.2 – Laminar flow biological safety cabinets (Class II) for personnel and environmental protection; clauses 5.1.5 and 5.1.6
- AS 2252.6 – Clean workstations – design, installation and use
- AS 2567 – Laminar flow cytotoxic drug safety cabinets; clauses 5.1.5 and 5.1.6 only
- ISO 14644-1 – Cleanrooms and associated controlled environments – classification and air cleanliness
- AS/NZS 14644.2 – Specifications for testing and monitoring to prove continued compliance with ISO 14644-1 (ISO 14644-2:2000, MOD)
- AS/NZS 14644.3 – Test methods (ISO 14644-3:2005, MOD)
- ISO 14644-3 – Cleanrooms and associated controlled environments part 3: test methods
- BS EN 12469 – Biotechnology – Performance criteria for microbiological safety cabinets
- NSF 49 – Class II (Laminar flow) Biohazard Cabinetry, Annex F – Field Tests
Biological Condition 1.71
Sampling in accordance with in-house method TP029 based on ALPHA Compendium of methods for the Microbiologcal Examination of Foods, 5th ED., 3.102
- Air (Impaction Method) for Yeast, Mould and Aerobic (Bacteria)
Analysis of samples collected are performed by another IANZ accredited Laboratory
New Zealand