We support our customers with tailored consultancy packages to help guide them through GMP compliance and the complexities of validation and qualification of their facilities and equipment. Supporting customers at each stage of a project, from initial URS preparation through all the qualification steps and into PQ. We provide support with critical validation documentation preparation, implementation and execution.

  • User Requirement Specifications (URS)
  • Validation Master Plans (VMP)
  • Tender Proposal Evaluations
  • Enhanced Design Reviews – Design Qualification (DQ)
  • Factory Acceptance Tests (FAT)
  • Site Acceptance Tests (SAT)
  • Installation Qualification (IQ)
  • Operational Qualification (OQ)
  • Performance Qualification (PQ)
  • Validation Summary Reports (VSR)

Our gap analysis studies and audit investigations address existing systems, equipment and validation documentation. They allow customers to understand where any shortfalls may exist in their systems or procedures.

Our consultancy service can also offer bespoke training packages on specific aspects including basic contamination control, cleanroom design & construction, current & proposed cleanroom standards, cleanroom changing procedures and engineering support for clean areas

Our Services

Every industry includes operations that demand cleanroom or contamination-controlled
environments. That’s where Validair’s expertise delivers.

Testing & Verification


Supporting Services


“We set out to be the quality choice because our quality is the best. The evidence is in our ISO 9001 accreditation and ISO 17025 UKAS certification as well as our ethos to meet and exceed customer expectations. But more than that, we always do what we came to do. That is a vital part of delivering the very best quality service.”
STEVE WARD, Managing Director

Talk to Us

Please get in touch to discuss your exact requirements and allow us to offer the best solutions.

Contact Us