Validation for controlled environments and critical spaces

Operation theatres, cleanrooms, laminar flow cabinets and biosafety cabinets — validated against ISO/IEC 17025:2017-compliant test parameters, with NABL-accredited certification.

Technician entering a sterile validated cleanroom

Where calibration ends, validation begins

Calibration confirms an instrument reads correctly. Validation confirms the environment it operates in — an operation theatre, cleanroom or biosafety cabinet — actually performs to the standard your patients, staff or products require. Vanavil carries out both, so hospitals and laboratories get one accountable provider for equipment and environment.

Our validation work follows ISO IEC 17025:2017 procedures and is backed by NABL accreditation.

Environments we validate

OT Validation

Operation theatre environmental validation for patient safety and infection control.

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Laminar Flow Validation

Airflow and filtration performance testing for laminar flow work stations.

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Biosafety Cabinet Validation

Containment and airflow verification, including UV sterilisation effectiveness.

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Cleanroom Validation

Full environmental qualification — particle counts, pressure differential, temperature & humidity.

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Temperature & Humidity Validation

Environmental monitoring validation for storage and controlled areas.

Pass Box Testing

Interlocking and air integrity testing for material transfer pass boxes.

PCR Hood Testing

Performance testing for PCR hoods used in molecular diagnostic workflows.

What we measure during validation

Applied across OT, cleanroom, laminar flow and biosafety cabinet validation as relevant to each environment.

Maintains clean air quality in operation theatres and cleanrooms by verifying particle concentration against the required classification. See our dedicated Particle Count Testing page for full technical scope.
Tests ventilation to confirm proper, even airflow across the workspace or room. Related: Airflow & ACPH Testing and Laminar Air Flow Testing.
Ensures HEPA filters are functioning effectively with no leaks or degradation. Full details on our HEPA Filter Integrity Testing page.
Balances positive and negative air pressures between adjoining spaces to control contamination flow.
Verifies optimal environmental conditions are maintained within the validated space.
Tests lighting levels for precision surgical and procedural work.
Assesses noise levels to help maintain a controlled, tranquil environment where required.
Verifies the effectiveness of UV sterilisation in biosafety cabinets and laminar flow units.

A structured path to a compliant environment

  • Site assessment and test-parameter scoping
  • On-site testing against ISO IEC 17025:2017 procedures
  • Documented validation report with pass/fail results per parameter
  • Recommendations for any corrective action required
Technician monitoring cleanroom validation readings

Who relies on our validation work

Hospitals

Operation theatres and critical care environments.

Laboratories

Diagnostic and research cleanroom spaces.

Industrial Facilities

Controlled manufacturing environments.

One accredited provider, full accountability

  • NABL Certificate of Accreditation
  • ISO IEC 17025:2017-compliant test procedures
  • Calibration and validation from the same technical team
  • Reports structured for audit and regulatory review
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Duration depends on the number of parameters tested and the size of the space. We confirm a schedule once we understand the scope of your environment.
Yes, both are commonly validated in the same visit where they share test parameters such as airflow velocity and filter integrity.
They address different things — calibration confirms instrument accuracy, validation confirms the environment performs to standard. Most regulated facilities need both.

Ready to validate your facility?

Tell us which environments need validation and we'll scope the test parameters and schedule.