Cleanroom qualification and testing

Our team will assess your needs to build a custom testing schedule. To determine the most appropriate cleanroom validation tests, we’ll consider factors such as:

  • ISO standard or GMP guideline requirements
  • Validation frequency requirements, including annual and interim testing
  • Your URS, risk assessment, and monitoring plan

For GMP or pharma cleanroom commissioning, validations will have oversight from our regulatory governance team and tests will also depend on which cleanroom lifecycle phase needs qualification, including:

  • Installation Qualification (IQ) - meeting user and design requirements
  • Operational Qualification (OQ) – operating within the defined conditions
  • Performance Qualification (PQ) – in the operational state

Our cleanroom validation documentation is detailed and auditable. You will receive an interim report on the day of testing, followed readily by the full report. Reporting is aligned with ISO standards and GMP guidelines to meet your requirements and those of any nominated regulatory body, like the MHRA.

Validation tests

Scope for Testing

Validation testing

Connect 2 Cleanrooms' in-house team of experienced technicians is CTCB-i qualified to perform cleanroom qualification testing services. Our technicians have extensive cleanroom validation training and a wide range of qualifications to ensure they are technically competent to test and validate your cleanroom.

From running particle counts and air change testing on a small cleanroom to coordinating a full scope of testing on suites of cleanrooms within a planned maintenance period — we have the experience and expertise to manage your cleanroom validation effectively.

Our planning team will coordinate with you to ensure this critical service is completed efficiently, with minimal downtime for your process.

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Service Contracts

Validation agreements and service contracts

We can build a validation agreement to cover your validation requirements for a designated time period, i.e. 3 years. They can include servicing of HVAC to HTM03-01, as well as servicing of cleanrooms and bespoke clean air equipment such as laminar flow devices and air handling units.

The benefit of a validation agreement is that we can use year-on-year data to make recommendations and generate a cycle of continuous improvement. It also helps you budget for critical spares and planned maintenance.

Service contracts are also available on Connect 2 Cleanrooms’ facilities to cover:

  • Annual and interim cleanroom validation
  • 24/7 telephone support from our CTCB-I qualified team
  • Call out visit with an agreed response time
  • Extended warranty options

We will work with you to provide the most appropriate level of support, to keep your critical process protected.

Speak to us about your validation requirements

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