Compressed Air Testing India | ISO 8573 | NABL Accredited

Auriga Research provides NABL-accredited compressed air quality testing for pharmaceutical, food, hospital, and industrial users across India. Our field teams sample compressed air directly at the point of use and test for dew point, oil aerosol content, particulate concentration, and viable microbial counts per the ISO 8573 series of standards.

Periodic testing is required because compressed air picks up contamination from three sources — particulate matter from the ambient air drawn into the compressor, oil and wear products from the compressor itself, and rust, scale, and microbial growth from distribution piping and storage receivers. Unchecked contamination damages downstream equipment, fails GMP audits, and can compromise the safety of the finished product.

Parameters and Methods

Each parameter is mapped to its ISO 8573 sub-part so QA and validation teams can match scope to the required purity class at a glance.

ISO 8573-3

Dew Point

Water vapour content measured by chilled-mirror / digital hygrometer per ISO 8573-3.

ISO 8573-2

Oil Aerosol

Oil aerosol capture on membrane filter with gravimetric / GC-FID quantification per ISO 8573-2.

ISO 8573-5

Total Oil

Total oil content (aerosol + vapour) per ISO 8573-5 for pharma point-of-use compliance.

ISO 8573-4

Particulates

Particle concentration and size-distribution measurement per ISO 8573-4.

ISO 8573-7

Microbial Count

Total viable microbial count plus yeast and mould by impinger / contact plate per ISO 8573-7.

ISO 8573-6

Gaseous Contaminants

CO, CO₂, SO₂, NOx and other gaseous contaminants per ISO 8573-6.

ISO 8573-1

Purity Class

Reporting against ISO 8573-1 purity classes (e.g. Class 1.2.1 for pharma point-of-use).

Sources of Compressed Air Contamination

  • Particulates and aerosols from the ambient air drawn into the compressor intake
  • Oil mist and wear-metal particles introduced by the compressor itself and from lubricating oils
  • Water vapour condensing in receivers and distribution piping
  • Rust, scale, and pipe-wall debris from corroded or aged piping
  • Microbial growth — bacteria, yeasts, and moulds — proliferating in standing condensate

Who Needs Compressed Air Testing

  • Pharmaceutical manufacturers — Schedule M, WHO GMP, EU Annex 1 compliance
  • Food and beverage production lines using compressed air for packaging, filling, or product contact
  • Hospitals — medical air systems under HTM 02-01 / NABH requirements
  • Dairies, breweries, and distilleries
  • Cosmetics, nutraceutical, and herbal product manufacturers
  • Electronics, semiconductor, and precision cleanroom operations
  • Power plants, petroleum refineries, sugar mills, and other heavy industry protecting downstream equipment
  • Hotels and large facilities maintaining utility air quality

Sampling and Field Service

Our trained sampling engineers visit the site with calibrated ISO 8573-compliant sampling probes, digital hygrometers, particle counters, and microbial samplers. Samples are drawn at the point of use — typically immediately downstream of the final filter and at product-contact lines. Sampling locations, line pressures, flow rates, ambient conditions, and stabilisation times are documented for each test point.

Turnaround Time

On-site sampling at a single facility typically takes one working day. Dew point and particulate readings are captured in the field; oil aerosol and microbial samples are returned to the laboratory and analysed within 5-7 working days. The complete NABL-accredited compressed air quality report — including ISO 8573 purity class assignment for each test point — is delivered within 10-12 working days of sampling. Expedited reporting is available for urgent audit submissions.

Frequently Asked Questions

What standard governs compressed air quality testing?
Compressed air quality is governed by the ISO 8573 series of standards, which define purity classes for particles, water vapour (dew point), oil content, and microbial contamination. ISO 8573-1 specifies the air quality classes, while ISO 8573-2 through 8573-9 prescribe the sampling and test methods for each contaminant. Auriga Research follows ISO 8573-1 to 8573-9 protocols and reports results against the purity class required for your application — typical pharma point-of-use requires Class 1 or Class 2 air for particulates, water, and oil.
How is compressed air sampled at the point of use?
Samples are drawn from a calibrated sampling port immediately downstream of the point of use — at filling lines, contact-with-product piping, or critical utility outlets. Particulate and oil aerosol samples are collected on membrane filters using ISO 8573-2 / ISO 8573-4 sampling probes. Dew point is measured directly with calibrated chilled-mirror or digital hygrometer sensors. Microbial samples are collected onto agar contact plates or impinger solutions per ISO 8573-7. Sampling lines, flow rates, and stabilisation times are documented for each location.
What is the turnaround time for a compressed air quality report?
On-site sampling at a single facility typically takes one working day for multiple test points. Dew point and particulate readings are recorded in the field. Oil aerosol and microbial samples are couriered to the lab and analysed within 5-7 working days. A complete NABL-accredited compressed air quality report — with results compared against ISO 8573 purity classes — is issued within 10-12 working days of sampling completion.
Why is compressed air testing required for pharmaceutical manufacturing?
Compressed air in pharmaceutical facilities is classified as a critical utility under WHO GMP, Schedule M, and EU Annex 1. Where compressed air contacts product, primary packaging, or product-contact surfaces, manufacturers must demonstrate that the air meets a defined ISO 8573 purity class for particles, water, oil, and viable microbial counts. Periodic testing is mandatory and forms part of GMP audit evidence. Regulators including CDSCO, USFDA, and MHRA expect documented compressed air quality data at each point of use.
Which industries need compressed air quality testing?
Pharmaceutical manufacturing, food and beverage production, dairy, breweries and distilleries, hospital medical air systems, electronics and semiconductor cleanrooms, cosmetics, nutraceuticals, paint and coatings, and any operation where compressed air contacts product. Testing is also required for general industrial users seeking to protect downstream equipment from oil, water, and particulate contamination.

Get Your Compressed Air Quality Report

NABL-accredited compressed air testing per ISO 8573. On-site sampling and lab analysis for pharma, food, hospital, and industrial users.

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