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HVAC, cleanroom & healthcare engineering · Ahmedabad

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HVAC · Cleanrooms · HealthcareA-01

Turnkey HVAC & cleanroom engineering for critical environments

Design, execution, commissioning, validation and lifecycle support for regulated facilities in Ahmedabad, delivered under a single contract, with the IQ/OQ/PQ testing that proves it.

Built for
Pharmaceutical · Hospitals · Precision manufacturing
Designed and tested to
ISO 14644-1 · WHO-GMP · USFDA · NABH

ServicesA-02

Five disciplines, carried under one contract

Each of these is a full scope we deliver ourselves, from calculation through to the test record. Most projects use more than one, which is the reason they are not sold separately.

ProcessA-04

Requirement to handover, in five phases

Each phase closes on a document before the next one opens. That sequence is what makes the last phase possible at all. A performance result on an installation that was never formally verified cannot be defended in an audit.

  1. 01

    Requirement

    What the rooms have to hold, what happens inside them, and which standard governs. Usually from a layout, a URS or a walk-through of the existing facility.

    Requirement summary and applicable standard

  2. 02

    Engineering & Design

    Heat load, air volumes, classification and pressure relationships are calculated first. Equipment, ducting and enclosure are selected from those numbers, not before them.

    Design package, drawings and equipment schedule

  3. 03

    Execution

    Fabrication, installation and site coordination for the HVAC and the enclosure together, phased around whatever else is happening in the building.

    Installed system and as-built drawings

  4. 04

    Testing & Validation

    Balanced first, then measured: velocities, air changes, differential pressures, filter integrity, temperature and humidity, each recorded against a location and a date.

    Test records and IQ/OQ/PQ documentation

  5. 05

    Handover & AMC

    Documentation handed over, operators shown the system, and a maintenance scope agreed that keeps the rooms in the state they were signed off in.

    Handover file and maintenance schedule

Why AirvonA-05

What single-contract delivery actually changes

Most facility problems we are called in to fix are handover problems: the consultant drew it, someone else built it, and nobody owned the gap between the two.

  • 01

    Single-point accountability

    Design, execution, commissioning and support are coordinated through one engineering team. There is no gap between the consultant who drew it and the contractor who built it, because they are the same people.

  • 02

    Documentation-driven delivery

    The qualification requirement is fixed at design stage and carried through, so the paperwork an auditor asks for is produced by the project rather than assembled after it.

  • 03

    Tested before handover

    Systems are balanced, measured and recorded before completion. Velocities, air changes, differential pressures and filter integrity are figures on a page, not assurances.

  • 04

    Lifecycle support

    Rooms drift out of qualification quietly. AMC and retrofit scopes are built around filter management, rebalancing and re-qualification, so the facility keeps holding what it was signed off holding.

Start a projectA-07

Have a layout, URS or BOQ? Send it to our engineering team.

Area, classification if you know it, and what happens inside the room is enough to start. If the building does not exist yet, the architectural plan is enough.

Or call us directly. Most projects start on the phone

What happens next

  1. 01

    An engineer reads it

    Not a form handler. Within one working day.

  2. 02

    We ask three or four questions

    Usually the ones that decide the whole design, before they decide the cost.

  3. 03

    You get a written scope

    With the standards it would be built against. No cost, no obligation.