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    Clean Utilities.
    Compliant Operations.

    From compressed air to pure steam, Prewel Labs ensures your utilities meet the strictest pharma, medical device, and food safety standards.

    Why Test Utilities?

    Utilities like compressed air, gases, and steam are the hidden backbone of pharmaceutical, food, and healthcare operations.

    If their quality is compromised, it can:

    • Contaminate products and entire batches
    • Lead to regulatory non-compliance and audit failures
    • Cause costly recalls or production shutdowns
    • Put patient and consumer safety at serious risk
    Utilities Quality Testing

    Regular Utilities Testing Helps You Ensure:

    high-pressure tank with cap

    Regular Utilities Testing Helps You Ensure:

    • Compliance with GMP, ISO, USP, and other regulatory norms
    • Reliable and consistent performance of production systems
    • Reduced risk of contamination and non-conformance
    • Peace of mind during audits and inspections

    Types of Utility Testing We Provide

    Compressed Air Testing

    Compressed Air Testing

    Why : Contaminated air comes into direct or indirect contact with products and can ruin batches.

    What we test : Particulate matter, microbial load, dew point, oil aerosols, moisture content.

    Who needs it : Pharma, medical device, and food & beverage plants.

    Gas Testing

    Gas Testing (Process & Medical)

    Why : Gases like nitrogen, oxygen, and CO2 must meet strict purity standards.

    What we test : Purity, identity, hydrocarbons, moisture, microbial contamination.

    Who needs it : Pharma, biotech, medical gas suppliers, hospitals, F&B industry.

    Pure & Clean Steam Testing

    Pure & Clean Steam Testing

    Why : Steam used in sterilization and CIP systems must be free of contaminants.

    What we test : Non condensable gases, superheat, dryness fraction, conductivity, microbes.

    Who needs it : Pharma, biotech, and medical device sterilization units.

    Benefits of Testing with Prewel Labs

    Compliance Assurance

    Meet GMP, USP, ISO, and pharmacopeia standards.

    Risk Prevention

    Detect contamination before it reaches production or patients.

    Audit Readiness

    Digital, audit ready reports accessible anytime.

    Specialist Expertise

    Utilities testing designed for pharma, med tech, and F& industries.

    Digital Dashboard

    Real time insights and AI foresight for proactive risk management.

    Benefits of Utilities Testing

    Who We Serve

    Pharma & Biopharma Plants

    Utilities for sterile and non sterile operations

    Medical Device Manufacturers

    Cleaning, sterilization, and compressed air testing

    Food & Beverage Companies

    Safe gases and compressed air for production line

    Hospitals & Healthcare

    Medical gases and sterilization steam

    Utilities Testing at a Glance

    Utility TypeWhy It MattersKey ParametersWho Needs It
    Compressed Air Prevents microbial & particulate contamination Particulates, dew point, oil aerosols, microbesPharma, med tech, F&B
    Process & Medical Gases Ensures purity & product safety Identity, purity, hydrocarbons, microbesPharma, hospitals, F&B
    Pure & Clean Steam Validates sterilization & CIP systems NCG, dryness, superheat, conductivity, microbes Pharma, med tech, healthcare

    The Utilities You Don’t See Can Make or Break Compliance.

    Prewel Labs ensures your compressed air, gases, and steam are pure, compliant, and audit ready.

    FAQs

    Utilities testing ensures that compressed air, gases, and steam used in production, cleaning, or sterilization processes do not introduce chemical, physical, or microbial contaminants into products or equipment.

    Frequency depends on risk and regulatory expectations, but most facilities follow:

    • Compressed Air: Quarterly or bi-annually
    • Process/Medical Gases: Annually
    • Pure Steam: Bi-annually or annually or after major maintenance
      A custom schedule can be created based on your QMS or audit history.

    We offer both options:

    • Our trained technicians can visit your facility for onsite sampling, or
    • Your team can collect samples following our validated sampling procedure.

    Yes. Many parameters such as microbial air sampling, dew point, NCG measurement, and steam dryness can be performed onsite to avoid delays and ensure immediate corrective action.

    We use calibrated and traceable instruments such as laser particle counters, dew point meters, oil aerosol detectors, microbial air samplers, and steam quality test kits compliant with USP, EN, ISO, and IS standards.

    Utilities testing is essential in:

    • Medical device manufacturing
    • Pharmaceutical manufacturing
    • Food & beverage plants
    • Cosmetics industry
    • Biotech R&D facilities
    • Hospitals & sterile processing departments

    Most onsite utility testing is completed within 2–4 hours, depending on the number of sampling points.
    Microbial results may take 48–72 hours.

    No. Sampling is designed to be non-intrusive, and most tests can be carried out without shutting down production, unless your SOPs require isolation.

    You receive a comprehensive report including:

    • Raw data
    • Instrument calibration certificates
    • Photographs of sampling points
    • Deviation observations (if any)
    • Interpretation based on regulatory limits

    Yes. Our experts provide root cause analysis (RCA) and recommend corrective actions such as filter replacement, desiccant regeneration, pipeline sanitization, or system redesign.

    Yes. We provide onsite compressed air, gas purity, and steam quality testing across all major industrial hubs in India, including:
    Bengaluru, Hyderabad, Chennai, Mumbai, Pune, Goa, Ahmedabad, Delhi, and more.

    Yes. We support international clients through:

    • Sample shipment (where applicable)
    • Virtual audits
    • Onsite visits through partner laboratories
    • Compliance reports aligned with global standards (USP, EP, ISO, IS, BS)

    We comply with:

    • ISO 8573 (for compressed air)
    • EN 285 (for steam sterilizers)
    • Pharmacopeias (IP, EP, USP)
    • GMP & WHO TRS guidelines

    Some frequent issues include:

    • Oil carryover from compressors
    • Damaged or saturated filters
    • Moisture build-up
    • Rust or scale in pipelines
    • Ineffective sterilizer steam traps
    • Poor gas cylinder handling
      We assist in identifying and correcting these problems.
    • Most physical parameters: Same day
    • Chemical parameters: 24–48 hours
    • Microbiology: 48–72 hours
      Emergency TAT can be provided for critical operations.

    Absolutely. We support clients in designing a sampling point layout based on risk level, pipeline length, point-of-use criticality, and regulatory expectations.

    We help identify sources such as wet receivers, rust, damaged filters, or backflow, and guide corrective measures like sanitization, filter upgrades, or drain redesign.

    Yes. We assist in preparing URS, sampling SOPs, maintenance SOPs, and PQ protocols for utilities.

    Yes. We test blended gases such as carbogen, nitrous oxide mixtures, and special welding blends used in pharma and medical device manufacturing.

    Yes. Moisture in gases is assessed using detector tubes, moisture analyzers, or trace moisture sensors depending on accuracy requirements.